메뉴 건너뛰기




Volumn , Issue , 2009, Pages 99-123

Antenatal Diagnosis

Author keywords

Analysis of free fetal DNA (ffDNA) present in maternal blood; Antenatal diagnosis; Chorionic villus sampling prenatal diagnostic test; Inherited bleeding disorders affecting daily life and psychological wellbeing; Pre implantation genetic diagnosis (PGD); Prenatal diagnosis of hemophilia; Prenatal diagnostic techniques; Reproductive options for women with inherited bleeding disorders; sperm sorting alternative approach for women with X linked disorders; Von Willebrand disease (VWD) autosomal condition affecting males and females

Indexed keywords


EID: 84880590190     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781444303490.ch9     Document Type: Chapter
Times cited : (3)

References (205)
  • 1
    • 0023164845 scopus 로고
    • Epidemiological investigation of the prevalence of von Willebrand's disease
    • Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood 1987; 69: 454-459.
    • (1987) Blood , vol.69 , pp. 454-459
    • Rodeghiero, F.1    Castaman, G.2    Dini, E.3
  • 2
    • 0027458101 scopus 로고
    • Prevalence of von Willebrand disease in children: a multiethnic study
    • Werner EJ, Broxson EH, Tucker EL, et al. Prevalence of von Willebrand disease in children: a multiethnic study. J Pediatr 1993; 123: 893-898.
    • (1993) J Pediatr , vol.123 , pp. 893-898
    • Werner, E.J.1    Broxson, E.H.2    Tucker, E.L.3
  • 5
    • 34548405957 scopus 로고    scopus 로고
    • Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review
    • Mujezinovic F, Alfirevic Z. Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review. Obstet Gynecol 2007; 110: 687-694.
    • (2007) Obstet Gynecol , vol.110 , pp. 687-694
    • Mujezinovic, F.1    Alfirevic, Z.2
  • 6
    • 0028258978 scopus 로고
    • Analysis of limb reduction defects in babies exposed to chorionic villus sampling
    • Firth HV, Boyd PA, Chamberlain PF, et al. Analysis of limb reduction defects in babies exposed to chorionic villus sampling. Lancet 1994; 343: 1069-1071.
    • (1994) Lancet , vol.343 , pp. 1069-1071
    • Firth, H.V.1    Boyd, P.A.2    Chamberlain, P.F.3
  • 7
    • 84889616673 scopus 로고    scopus 로고
    • RCOG. Amniocentesis and chorionic villus sampling. Guideline No. 8
    • RCOG. Amniocentesis and chorionic villus sampling. Guideline No. 8. 2005.
    • (2005)
  • 8
    • 0022650629 scopus 로고
    • Randomised controlled trial of genetic amniocentesis in 4606 low-risk women
    • Tabor A, Philip J, Madsen M et al. Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet 1986; 1: 1287-1293.
    • (1986) Lancet , vol.1 , pp. 1287-1293
    • Tabor, A.1    Philip, J.2    Madsen, M.3
  • 9
    • 0032562014 scopus 로고    scopus 로고
    • Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis
    • The Canadian Early and Mid-trimester Amniocentesis Trial (CEMATGroup)
    • The Canadian Early and Mid-trimester Amniocentesis Trial (CEMATGroup). Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis. Lancet 1998; 351: 242-247.
    • (1998) Lancet , vol.351 , pp. 242-247
  • 10
    • 0034880961 scopus 로고    scopus 로고
    • Risk of fetal loss in twin pregnancies undergoing second trimester amniocentesis (1)
    • Yukobowich E, Anteby EY, Cohen SM, et al. Risk of fetal loss in twin pregnancies undergoing second trimester amniocentesis (1). Obstet Gynecol 2001; 98: 231-234.
    • (2001) Obstet Gynecol , vol.98 , pp. 231-234
    • Yukobowich, E.1    Anteby, E.Y.2    Cohen, S.M.3
  • 12
    • 0032857502 scopus 로고    scopus 로고
    • Elective cytogenetic amniocentesis in the third trimester for pregnancies with high risk factors
    • Shalev J, Meizner I, Rabinerson D, et al. Elective cytogenetic amniocentesis in the third trimester for pregnancies with high risk factors. Prenat Diagn 1999; 19: 749-752.
    • (1999) Prenat Diagn , vol.19 , pp. 749-752
    • Shalev, J.1    Meizner, I.2    Rabinerson, D.3
  • 13
    • 0036086685 scopus 로고    scopus 로고
    • [Third trimester amniocentesis for fetal karyotyping: why so late?.]
    • Rozenberg P. [Third trimester amniocentesis for fetal karyotyping: why so late?.]. Gynecol Obstet Fertil 2002; 30: 427-430.
    • (2002) Gynecol Obstet Fertil , vol.30 , pp. 427-430
    • Rozenberg, P.1
  • 14
    • 0020036125 scopus 로고
    • Complications of amniocentesis: a review
    • Galle PC, Meis PJ. Complications of amniocentesis: a review. J Reprod Med 1982; 27: 149-155.
    • (1982) J Reprod Med , vol.27 , pp. 149-155
    • Galle, P.C.1    Meis, P.J.2
  • 15
    • 0036152805 scopus 로고    scopus 로고
    • Complications of third-trimester amniocentesis using continuous ultrasound guidance
    • Gordon MC, Narula K, O'Shaughnessy R, Barth WH, Jr. Complications of third-trimester amniocentesis using continuous ultrasound guidance. Obstet Gynecol 2002; 99: 255-259.
    • (2002) Obstet Gynecol , vol.99 , pp. 255-259
    • Gordon, M.C.1    Narula, K.2    O'Shaughnessy, R.3    Barth, Jr.W.H.4
  • 16
    • 0033988384 scopus 로고    scopus 로고
    • Need for urgent delivery after third-trimester amniocentesis
    • Stark CM, Smith RS, Lagrandeur RM, et al. Need for urgent delivery after third-trimester amniocentesis. Obstet Gynecol 2000; 95: 48-50.
    • (2000) Obstet Gynecol , vol.95 , pp. 48-50
    • Stark, C.M.1    Smith, R.S.2    Lagrandeur, R.M.3
  • 17
    • 33646049049 scopus 로고    scopus 로고
    • Risk of thirdtrimester amniocentesis: a case-control study
    • Hodor JG, Poggi SH, Spong CY, et al. Risk of thirdtrimester amniocentesis: a case-control study. Am J Perinatol 2006; 23: 177-180.
    • (2006) Am J Perinatol , vol.23 , pp. 177-180
    • Hodor, J.G.1    Poggi, S.H.2    Spong, C.Y.3
  • 18
    • 0031968758 scopus 로고    scopus 로고
    • Clinical significance of amniotic-fluid-cell culture failure
    • Lam YH, Tang MH, Sin SY, Ghosh A. Clinical significance of amniotic-fluid-cell culture failure. Prenat Diagn 1998; 18: 343-347.
    • (1998) Prenat Diagn , vol.18 , pp. 343-347
    • Lam, Y.H.1    Tang, M.H.2    Sin, S.Y.3    Ghosh, A.4
  • 19
    • 34748902610 scopus 로고    scopus 로고
    • Amniocentesis in the third trimester of pregnancy
    • O'Donoghue K, Giorgi L, Pontello V, et al. Amniocentesis in the third trimester of pregnancy. Prenat Diagn 2007; 27: 1000-1004.
    • (2007) Prenat Diagn , vol.27 , pp. 1000-1004
    • O'Donoghue, K.1    Giorgi, L.2    Pontello, V.3
  • 20
    • 0029051986 scopus 로고
    • Cordocentesis for rapid karyotype: 421 consecutive cases
    • Donner C, Rypens F, Paquet V, et al. Cordocentesis for rapid karyotype: 421 consecutive cases. Fetal Diagn Ther 1995; 10: 192-199.
    • (1995) Fetal Diagn Ther , vol.10 , pp. 192-199
    • Donner, C.1    Rypens, F.2    Paquet, V.3
  • 21
    • 0030063799 scopus 로고    scopus 로고
    • Percutaneous umbilical blood sampling: indication changes and procedure loss rate in a nine years' experience
    • Buscaglia M, Ghisoni L, Bellotti M, et al. Percutaneous umbilical blood sampling: indication changes and procedure loss rate in a nine years' experience. Fetal Diagn Ther 1996; 11: 106-113.
    • (1996) Fetal Diagn Ther , vol.11 , pp. 106-113
    • Buscaglia, M.1    Ghisoni, L.2    Bellotti, M.3
  • 22
    • 0029982004 scopus 로고    scopus 로고
    • Diagnostic fetal blood samplingtechnique related losses
    • Weiner CP, Okamura K. Diagnostic fetal blood samplingtechnique related losses. Fetal Diagn Ther 1996; 11: 169-175.
    • (1996) Fetal Diagn Ther , vol.11 , pp. 169-175
    • Weiner, C.P.1    Okamura, K.2
  • 23
    • 0034035526 scopus 로고    scopus 로고
    • Cordocentesis at 16-24 weeks of gestation: experience of 1320 cases
    • Tongsong T, Wanapirak C, Kunavikatikul C, et al. Cordocentesis at 16-24 weeks of gestation: experience of 1320 cases. Prenat Diagn 2000; 20: 224-228.
    • (2000) Prenat Diagn , vol.20 , pp. 224-228
    • Tongsong, T.1    Wanapirak, C.2    Kunavikatikul, C.3
  • 24
    • 0035077023 scopus 로고    scopus 로고
    • Fetal loss rate associated with cordocentesis at midgestation
    • Tongsong T, Wanapirak C, Kunavikatikul C, et al. Fetal loss rate associated with cordocentesis at midgestation. Am J Obstet Gynecol 2001; 184: 719-723.
    • (2001) Am J Obstet Gynecol , vol.184 , pp. 719-723
    • Tongsong, T.1    Wanapirak, C.2    Kunavikatikul, C.3
  • 25
    • 33645915439 scopus 로고    scopus 로고
    • Efficacy and safety of cordocentesis for prenatal diagnosis
    • Liao C, Wei J, Li Q, et al. Efficacy and safety of cordocentesis for prenatal diagnosis. Int J Gynaecol Obstet 2006; 93: 13-17.
    • (2006) Int J Gynaecol Obstet , vol.93 , pp. 13-17
    • Liao, C.1    Wei, J.2    Li, Q.3
  • 26
    • 0025030753 scopus 로고
    • The risks of early cordocentesis (12-21 weeks): analysis of 500 procedures
    • Orlandi F, Damiani G, Jakil C, et al. The risks of early cordocentesis (12-21 weeks): analysis of 500 procedures. Prenat Diagn 1990; 10: 425-428.
    • (1990) Prenat Diagn , vol.10 , pp. 425-428
    • Orlandi, F.1    Damiani, G.2    Jakil, C.3
  • 28
    • 0025745093 scopus 로고
    • Fetal blood sampling and pregnancy loss in relation to indication
    • Maxwell DJ, Johnson P, Hurley P, et al. Fetal blood sampling and pregnancy loss in relation to indication. Br J Obstet Gynaecol 1991; 98: 892-897.
    • (1991) Br J Obstet Gynaecol , vol.98 , pp. 892-897
    • Maxwell, D.J.1    Johnson, P.2    Hurley, P.3
  • 29
    • 0028415082 scopus 로고
    • [Risk factors of fetal blood sampling. The essential risk is its duration]
    • Daffos F, Forestier F, Capella-Pavlovsky M, et al. [Risk factors of fetal blood sampling. The essential risk is its duration]. Rev Prat 1994; 44: 923-926.
    • (1994) Rev Prat , vol.44 , pp. 923-926
    • Daffos, F.1    Forestier, F.2    Capella-Pavlovsky, M.3
  • 30
    • 0027787872 scopus 로고
    • Complications of diagnostic ultrasound-guided percutaneous umbilical blood sampling: analysis of a series of cases and review of the literature
    • Duchatel F, Oury JF, Mennesson B, Muray JM. Complications of diagnostic ultrasound-guided percutaneous umbilical blood sampling: analysis of a series of cases and review of the literature. Eur J Obstet Gynecol Reprod Biol 1993; 52: 95-104.
    • (1993) Eur J Obstet Gynecol Reprod Biol , vol.52 , pp. 95-104
    • Duchatel, F.1    Oury, J.F.2    Mennesson, B.3    Muray, J.M.4
  • 31
    • 0024188897 scopus 로고
    • Diagnosis and treatment of feto-maternal hemorrhage in a fetus with homozygous von Willebrand's disease
    • Ash KM, Mibashan RS, Nicolaides KH. Diagnosis and treatment of feto-maternal hemorrhage in a fetus with homozygous von Willebrand's disease. Fetal Ther 1988; 3: 189-191.
    • (1988) Fetal Ther , vol.3 , pp. 189-191
    • Ash, K.M.1    Mibashan, R.S.2    Nicolaides, K.H.3
  • 32
    • 0020611038 scopus 로고
    • Determination of fetal sex
    • Birnholz JC. Determination of fetal sex. N Engl J Med 1983; 309: 942-944.
    • (1983) N Engl J Med , vol.309 , pp. 942-944
    • Birnholz, J.C.1
  • 33
    • 0022345776 scopus 로고
    • Visualization of the fetal genitalia by ultrasonography: a review of the literature and analysis of its accuracy and ethical implications
    • Elejalde BR, de Elejalde MM, Heitman T. Visualization of the fetal genitalia by ultrasonography: a review of the literature and analysis of its accuracy and ethical implications. J Ultrasound Med 1985; 4: 633-639.
    • (1985) J Ultrasound Med , vol.4 , pp. 633-639
    • Elejalde, B.R.1    de Elejalde, M.M.2    Heitman, T.3
  • 34
    • 0033037877 scopus 로고    scopus 로고
    • The sonographic identification of fetal gender from 11 to weeks of gestation
    • Whitlow BJ, Lazanakis MS, Economides DL. The sonographic identification of fetal gender from 11 to weeks of gestation. Ultrasound Obstet Gynecol 1999; 13: 301-304.
    • (1999) Ultrasound Obstet Gynecol , vol.13 , pp. 301-304
    • Whitlow, B.J.1    Lazanakis, M.S.2    Economides, D.L.3
  • 35
    • 0032055594 scopus 로고    scopus 로고
    • Fetal sex determination by high resolution ultrasound in early pregnancy
    • Mielke G, Kiesel L, Backsch C, Erz W, Gonser M. Fetal sex determination by high resolution ultrasound in early pregnancy. Eur J Ultrasound 1998; 7: 109-114.
    • (1998) Eur J Ultrasound , vol.7 , pp. 109-114
    • Mielke, G.1    Kiesel, L.2    Backsch, C.3    Erz, W.4    Gonser, M.5
  • 37
    • 29544450593 scopus 로고    scopus 로고
    • Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy
    • Hyett JA, Gardener G, Stojilkovic-Mikic T, et al. Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy. Prenat Diagn 2005; 25: 1111-1116.
    • (2005) Prenat Diagn , vol.25 , pp. 1111-1116
    • Hyett, J.A.1    Gardener, G.2    Stojilkovic-Mikic, T.3
  • 38
    • 33746648992 scopus 로고    scopus 로고
    • Non-invasive diagnosis of fetal sex; utilisation of free fetal DNA in maternal plasma and ultrasound
    • Avent ND, Chitty LS. Non-invasive diagnosis of fetal sex; utilisation of free fetal DNA in maternal plasma and ultrasound. Prenat Diagn 2006; 26: 598-603.
    • (2006) Prenat Diagn , vol.26 , pp. 598-603
    • Avent, N.D.1    Chitty, L.S.2
  • 39
    • 0032993260 scopus 로고    scopus 로고
    • Early fetal gender determination
    • Benott B. Early fetal gender determination. Ultrasound Obstet Gynecol 1999; 13: 299-300.
    • (1999) Ultrasound Obstet Gynecol , vol.13 , pp. 299-300
    • Benott, B.1
  • 40
    • 0033065959 scopus 로고    scopus 로고
    • Biometrical threshold of biparietal diameter for certain fetal sex assignment by ultrasound
    • Mazza V, Contu G, Falcinelli C, et al. Biometrical threshold of biparietal diameter for certain fetal sex assignment by ultrasound. Ultrasound Obstet Gynecol 1999; 13: 308-311.
    • (1999) Ultrasound Obstet Gynecol , vol.13 , pp. 308-311
    • Mazza, V.1    Contu, G.2    Falcinelli, C.3
  • 41
    • 4644323246 scopus 로고    scopus 로고
    • Sonographic biometrical range of external genitalia differentiation in the first trimester of pregnancy: analysis of 2593 cases
    • Mazza V, Di Monte, I, Pati M, et al. Sonographic biometrical range of external genitalia differentiation in the first trimester of pregnancy: analysis of 2593 cases. Prenat Diagn 2004; 24: 677-684.
    • (2004) Prenat Diagn , vol.24 , pp. 677-684
    • Mazza, V.1    Di Monte, I.2    Pati, M.3
  • 42
    • 0342618532 scopus 로고    scopus 로고
    • Presence of fetal DNA in maternal plasma and serum
    • Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997; 350: 485-487.
    • (1997) Lancet , vol.350 , pp. 485-487
    • Lo, Y.M.1    Corbetta, N.2    Chamberlain, P.F.3
  • 43
    • 0026761240 scopus 로고
    • First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood
    • Elias S, Price J, Dockter M, et al. First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood. Lancet 1992; 340: 1033.
    • (1992) Lancet , vol.340 , pp. 1033
    • Elias, S.1    Price, J.2    Dockter, M.3
  • 44
    • 0028863599 scopus 로고
    • Prenatal diagnosis by use of fetal cells isolated from maternal blood
    • de la Cruz F, Shifrin H, Elias S, et al. Prenatal diagnosis by use of fetal cells isolated from maternal blood. Am J Obstet Gynecol 1995; 173: 1354-1355.
    • (1995) Am J Obstet Gynecol , vol.173 , pp. 1354-1355
    • de la Cruz, F.1    Shifrin, H.2    Elias, S.3
  • 45
    • 0031776160 scopus 로고    scopus 로고
    • Fetal cells in maternal blood: current and future perspectives
    • Hahn S, Sant R, Holzgreve W. Fetal cells in maternal blood: current and future perspectives. Mol Hum Reprod 1998; 4: 515-521.
    • (1998) Mol Hum Reprod , vol.4 , pp. 515-521
    • Hahn, S.1    Sant, R.2    Holzgreve, W.3
  • 46
    • 0027261159 scopus 로고
    • Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational age
    • Hamada H, Arinami T, Kubo T, et al. Fetal nucleated cells in maternal peripheral blood: frequency and relationship to gestational age. Hum Genet 1993; 91: 427-432.
    • (1993) Hum Genet , vol.91 , pp. 427-432
    • Hamada, H.1    Arinami, T.2    Kubo, T.3
  • 47
    • 0347898005 scopus 로고    scopus 로고
    • Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis
    • Lo YM, Tein MS, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet 1998; 62: 768-775.
    • (1998) Am J Hum Genet , vol.62 , pp. 768-775
    • Lo, Y.M.1    Tein, M.S.2    Lau, T.K.3
  • 48
    • 0036626528 scopus 로고    scopus 로고
    • Presence of fetal DNA in maternal plasma decades after pregnancy
    • Invernizzi P, Biondi ML, Battezzati PM, et al. Presence of fetal DNA in maternal plasma decades after pregnancy. Hum Genet 2002; 110: 587-591.
    • (2002) Hum Genet , vol.110 , pp. 587-591
    • Invernizzi, P.1    Biondi, M.L.2    Battezzati, P.M.3
  • 49
    • 33847239357 scopus 로고    scopus 로고
    • Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
    • Santacroce R, Vecchione G, Tomaiyolo M, et al. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Hemophilia 2006; 12: 417-422.
    • (2006) Hemophilia , vol.12 , pp. 417-422
    • Santacroce, R.1    Vecchione, G.2    Tomaiyolo, M.3
  • 50
    • 18744415967 scopus 로고    scopus 로고
    • Fetal DNA clearance from maternal plasma is impaired in preeclampsia
    • Lau TW, Leung TN, Chan LY, et al. Fetal DNA clearance from maternal plasma is impaired in preeclampsia. Clin Chem 2002; 48: 2141-2146.
    • (2002) Clin Chem , vol.48 , pp. 2141-2146
    • Lau, T.W.1    Leung, T.N.2    Chan, L.Y.3
  • 52
    • 0038620220 scopus 로고    scopus 로고
    • No evidence of fetal DNA persistence in maternal plasma after pregnancy
    • Smid M, Galbiati S, Vassallo A, et al. No evidence of fetal DNA persistence in maternal plasma after pregnancy. Hum Genet 2003; 112: 617-618.
    • (2003) Hum Genet , vol.112 , pp. 617-618
    • Smid, M.1    Galbiati, S.2    Vassallo, A.3
  • 53
    • 0036938305 scopus 로고    scopus 로고
    • Evidence against the long-term persistence of fetal DNA in maternal plasma after pregnancy
    • Johnson-Hopson CN, Artlett CM. Evidence against the long-term persistence of fetal DNA in maternal plasma after pregnancy. Hum Genet 2002; 111: 575.
    • (2002) Hum Genet , vol.111 , pp. 575
    • Johnson-Hopson, C.N.1    Artlett, C.M.2
  • 54
    • 0037594898 scopus 로고    scopus 로고
    • Fetal DNA in maternal serum: does it persist after pregnancy?
    • Benachi A, Steffann J, Gautier E, et al. Fetal DNA in maternal serum: does it persist after pregnancy?. Hum Genet 2003; 113: 76-79.
    • (2003) Hum Genet , vol.113 , pp. 76-79
    • Benachi, A.1    Steffann, J.2    Gautier, E.3
  • 55
    • 0033364339 scopus 로고    scopus 로고
    • Rapid clearance of fetal DNA from maternal plasma
    • Lo YM, Zhang J, Leung TN, et al. Rapid clearance of fetal DNA from maternal plasma. Am J Hum Genet 1999; 64: 218-224.
    • (1999) Am J Hum Genet , vol.64 , pp. 218-224
    • Lo, Y.M.1    Zhang, J.2    Leung, T.N.3
  • 56
    • 0030034519 scopus 로고    scopus 로고
    • Male fetal progenitor cells persist in maternal blood for as long as years postpartum
    • Bianchi DW, Zickwolf GK, Weil GJ, et al. Male fetal progenitor cells persist in maternal blood for as long as years postpartum. Proc Natl Acad Sci USA 1996; 93: 705-708.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 705-708
    • Bianchi, D.W.1    Zickwolf, G.K.2    Weil, G.J.3
  • 57
    • 0035684463 scopus 로고    scopus 로고
    • First-trimester fetal sex determination in maternal serum using realtime PCR
    • Costa JM, Benachi A, Gautier E, et al. First-trimester fetal sex determination in maternal serum using realtime PCR. Prenat Diagn 2001; 21: 1070-1074.
    • (2001) Prenat Diagn , vol.21 , pp. 1070-1074
    • Costa, J.M.1    Benachi, A.2    Gautier, E.3
  • 58
    • 0034821298 scopus 로고    scopus 로고
    • Accuracy of fetal gender determination by analysis of DNA in maternal plasma
    • Sekizawa A, Kondo T, Iwasaki M, et al. Accuracy of fetal gender determination by analysis of DNA in maternal plasma. Clin Chem 2001; 47: 1856-1858.
    • (2001) Clin Chem , vol.47 , pp. 1856-1858
    • Sekizawa, A.1    Kondo, T.2    Iwasaki, M.3
  • 59
    • 0036461167 scopus 로고    scopus 로고
    • Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum
    • Honda H, Miharu N, Ohashi Y, et al. Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum. Hum Genet 2002; 110: 75-79.
    • (2002) Hum Genet , vol.110 , pp. 75-79
    • Honda, H.1    Miharu, N.2    Ohashi, Y.3
  • 60
    • 0037341393 scopus 로고    scopus 로고
    • Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination
    • Hromadnikova I, Houbova B, Hridelova D, et al. Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination. Prenat Diagn 2003; 23: 235-238.
    • (2003) Prenat Diagn , vol.23 , pp. 235-238
    • Hromadnikova, I.1    Houbova, B.2    Hridelova, D.3
  • 61
    • 0346458745 scopus 로고    scopus 로고
    • Earliest gestational age for fetal sexing in cell-free maternal plasma
    • Rijnders RJ, Van Der Luijt RB, Peters ED, et al. Earliest gestational age for fetal sexing in cell-free maternal plasma. Prenat Diagn 2003; 23: 1042-1044.
    • (2003) Prenat Diagn , vol.23 , pp. 1042-1044
    • Rijnders, R.J.1    Van Der Luijt, R.B.2    Peters, E.D.3
  • 62
    • 0742333328 scopus 로고    scopus 로고
    • Clinical applications of cell-free fetal DNA from maternal plasma
    • Rijnders RJ, Christiaens GC, Bossers B, et al. Clinical applications of cell-free fetal DNA from maternal plasma. Obstet Gynecol 2004; 103: 157-164.
    • (2004) Obstet Gynecol , vol.103 , pp. 157-164
    • Rijnders, R.J.1    Christiaens, G.C.2    Bossers, B.3
  • 63
    • 0034818672 scopus 로고    scopus 로고
    • Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia
    • Rijnders RJ, van der Schoot CE, Bossers B, et al. Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia. Obstet Gynecol 2001; 98: 374-378.
    • (2001) Obstet Gynecol , vol.98 , pp. 374-378
    • Rijnders, R.J.1    van der Schoot, C.E.2    Bossers, B.3
  • 64
    • 0035107577 scopus 로고    scopus 로고
    • Risk free simultaneous prenatal identification of fetal Rhesus D status and sex by multiplex real-time PCR using cell free fetal DNA in maternal plasma
    • Zhong XY, Holzgreve W, Hahn S. Risk free simultaneous prenatal identification of fetal Rhesus D status and sex by multiplex real-time PCR using cell free fetal DNA in maternal plasma. Swiss Med Wkly 2001; 131: 70-74.
    • (2001) Swiss Med Wkly , vol.131 , pp. 70-74
    • Zhong, X.Y.1    Holzgreve, W.2    Hahn, S.3
  • 65
    • 0043124696 scopus 로고    scopus 로고
    • Kinetics of SRY gene appearance in maternal serum: detection by real time PCR in early pregnancy after assisted reproductive technique
    • Guibert J, Benachi A, Grebille AG, et al. Kinetics of SRY gene appearance in maternal serum: detection by real time PCR in early pregnancy after assisted reproductive technique. Hum Reprod 2003; 18: 1733-1736.
    • (2003) Hum Reprod , vol.18 , pp. 1733-1736
    • Guibert, J.1    Benachi, A.2    Grebille, A.G.3
  • 66
    • 3242670445 scopus 로고    scopus 로고
    • Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseases
    • Cremonesi L, Galbiati S, Foglieni B, et al. Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseases. Ann NY Acad Sci 2004; 1022: 105-112.
    • (2004) Ann NY Acad Sci , vol.1022 , pp. 105-112
    • Cremonesi, L.1    Galbiati, S.2    Foglieni, B.3
  • 67
    • 12944331281 scopus 로고    scopus 로고
    • Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation
    • Birch L, English CA, O'Donoghue K, et al. Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation. Clin Chem 2005; 51: 312-320.
    • (2005) Clin Chem , vol.51 , pp. 312-320
    • Birch, L.1    English, C.A.2    O'Donoghue, K.3
  • 68
    • 34548501087 scopus 로고    scopus 로고
    • Early detection of cell-free fetal DNA in maternal plasma
    • Illanes S, Denbow M, Kailasam C, et al. Early detection of cell-free fetal DNA in maternal plasma. Early Hum Dev 2007; 83: 563-566.
    • (2007) Early Hum Dev , vol.83 , pp. 563-566
    • Illanes, S.1    Denbow, M.2    Kailasam, C.3
  • 69
    • 0018130370 scopus 로고
    • Sampling pure fetal blood by fetoscopy in second trimester of pregnancy
    • Rodeck CH, Campbell S. Sampling pure fetal blood by fetoscopy in second trimester of pregnancy. BMJ 1978; 2: 728-730.
    • (1978) BMJ , vol.2 , pp. 728-730
    • Rodeck, C.H.1    Campbell, S.2
  • 70
    • 0018748499 scopus 로고
    • An immunoradiometric assay for procoagulant factor VIII antigen: results in haemophilia, von Willebrand's disease and fetal plasma and serum
    • Peake IR, Bloom AL, Giddings JC, Ludlam CA. An immunoradiometric assay for procoagulant factor VIII antigen: results in haemophilia, von Willebrand's disease and fetal plasma and serum. Br J Hematol 1979; 42: 269-281.
    • (1979) Br J Hematol , vol.42 , pp. 269-281
    • Peake, I.R.1    Bloom, A.L.2    Giddings, J.C.3    Ludlam, C.A.4
  • 71
    • 0019216022 scopus 로고
    • Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX
    • Holmberg L, Gustavii B, Cordesius E, et al. Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX. Blood 1980; 56: 397-401.
    • (1980) Blood , vol.56 , pp. 397-401
    • Holmberg, L.1    Gustavii, B.2    Cordesius, E.3
  • 73
    • 0018745699 scopus 로고
    • Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophilia
    • Mibashan RS, Rodeck CH, Thumpston JK, et al. Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophilia. Lancet 1979; 1: 1309-1311.
    • (1979) Lancet , vol.1 , pp. 1309-1311
    • Mibashan, R.S.1    Rodeck, C.H.2    Thumpston, J.K.3
  • 74
    • 0020960011 scopus 로고
    • A new procedure for fetal blood sampling in utero: preliminary results of fifty-three cases
    • Daffos F, Capella-Pavlovsky M, Forestier F. A new procedure for fetal blood sampling in utero: preliminary results of fifty-three cases. Am J Obstet Gynecol 1983; 146: 985-987.
    • (1983) Am J Obstet Gynecol , vol.146 , pp. 985-987
    • Daffos, F.1    Capella-Pavlovsky, M.2    Forestier, F.3
  • 75
    • 0020079806 scopus 로고
    • Ultrasound-guided fetal intravenous transfusion for severe rhesus haemolytic disease
    • Bang J, Bock JE, Trolle D. Ultrasound-guided fetal intravenous transfusion for severe rhesus haemolytic disease. BMJ (Clin Res Ed) 1982; 284: 373-374.
    • (1982) BMJ (Clin Res Ed) , vol.284 , pp. 373-374
    • Bang, J.1    Bock, J.E.2    Trolle, D.3
  • 76
    • 0021276777 scopus 로고
    • The results of the first meeting of the International Fetoscopy Group
    • The status of fetoscopy and fetal tissue sampling
    • The status of fetoscopy and fetal tissue sampling. The results of the first meeting of the International Fetoscopy Group. Prenat Diagn 1984; 4: 79-81.
    • (1984) Prenat Diagn , vol.4 , pp. 79-81
  • 77
    • 0021750055 scopus 로고
    • Characterization of the human factor VIII gene
    • Gitschier J, Wood WI, Goralka TM, et al. Characterization of the human factor VIII gene. Nature 1984; 312: 326-330.
    • (1984) Nature , vol.312 , pp. 326-330
    • Gitschier, J.1    Wood, W.I.2    Goralka, T.M.3
  • 78
    • 0022257323 scopus 로고
    • Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)
    • Yoshitake S, Schach BG, Foster DC, et al. Nucleotide sequence of the gene for human factor IX (antihemophilic factor B). Biochemistry 1985; 24: 3736-3750.
    • (1985) Biochemistry , vol.24 , pp. 3736-3750
    • Yoshitake, S.1    Schach, B.G.2    Foster, D.C.3
  • 79
    • 0020622897 scopus 로고
    • Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound
    • Ward RH, Modell B, Petrou M, et al. Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound. BMJ (Clin Res Ed) 1983; 286: 1542-1544.
    • (1983) BMJ (Clin Res Ed) , vol.286 , pp. 1542-1544
    • Ward, R.H.1    Modell, B.2    Petrou, M.3
  • 80
    • 0021268910 scopus 로고
    • Transabdominal fine needle biopsy from chorionic villi in the first trimester
    • Smidt-Jensen S, Hahnemann N. Transabdominal fine needle biopsy from chorionic villi in the first trimester. Prenat Diagn 1984; 4: 163-169.
    • (1984) Prenat Diagn , vol.4 , pp. 163-169
    • Smidt-Jensen, S.1    Hahnemann, N.2
  • 81
    • 0021876387 scopus 로고
    • Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe
    • Gitschier J, Lawn RM, Rotblat F, et al. Antenatal diagnosis and carrier detection of haemophilia A using factor VIII gene probe. Lancet 1985; 1: 1093-1094.
    • (1985) Lancet , vol.1 , pp. 1093-1094
    • Gitschier, J.1    Lawn, R.M.2    Rotblat, F.3
  • 82
    • 0024840950 scopus 로고
    • Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A
    • Chan V, Tong TM, Chan TP, et al. Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of haemophilia A. Br J Hematol 1989; 73: 497-500.
    • (1989) Br J Hematol , vol.73 , pp. 497-500
    • Chan, V.1    Tong, T.M.2    Chan, T.P.3
  • 83
    • 0023205847 scopus 로고
    • Hemophilia A: carrier detection and prenatal diagnosis by DNA analysis
    • Pecorara M, Casarino L, Mori PG, et al. Hemophilia A: carrier detection and prenatal diagnosis by DNA analysis. Blood 1987; 70: 531-535.
    • (1987) Blood , vol.70 , pp. 531-535
    • Pecorara, M.1    Casarino, L.2    Mori, P.G.3
  • 84
    • 0023624667 scopus 로고
    • Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A
    • Sampietro M, Camerino G, Romano M, et al. Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A. Thromb Haemost 1987; 58: 988-992.
    • (1987) Thromb Haemost , vol.58 , pp. 988-992
    • Sampietro, M.1    Camerino, G.2    Romano, M.3
  • 85
    • 0023713974 scopus 로고
    • First trimester prenatal diagnosis of haemophilia A: two years' experience
    • Brocker-Vriends AH, Briet E, Kanhai HH, et al. First trimester prenatal diagnosis of haemophilia A: two years' experience. Prenat Diagn 1988; 8: 411-421.
    • (1988) Prenat Diagn , vol.8 , pp. 411-421
    • Brocker-Vriends, A.H.1    Briet, E.2    Kanhai, H.H.3
  • 86
    • 0024997755 scopus 로고
    • Carrier detection and prenatal diagnosis in haemophilia A and B
    • Chistolini A, Papacchini M, Mazzucconi MG, et al. Carrier detection and prenatal diagnosis in haemophilia A and B. Hematologica 1990; 75: 424-428.
    • (1990) Hematologica , vol.75 , pp. 424-428
    • Chistolini, A.1    Papacchini, M.2    Mazzucconi, M.G.3
  • 87
    • 0026486091 scopus 로고
    • Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center
    • Sacchi E, Randi AM, Tagliavacca L, et al. Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center. Int J Clin Lab Res 1992; 21: 310-313.
    • (1992) Int J Clin Lab Res , vol.21 , pp. 310-313
    • Sacchi, E.1    Randi, A.M.2    Tagliavacca, L.3
  • 88
    • 0026149980 scopus 로고
    • Carrier detection and prenatal diagnosis in 98 families of haemophilia A by linkage analysis and direct detection of mutations
    • Lavergne JM, Laurian Y, Dudilleux A, et al. Carrier detection and prenatal diagnosis in 98 families of haemophilia A by linkage analysis and direct detection of mutations. Blood Coagul Fibrinolysis 1991; 2: 293-301.
    • (1991) Blood Coagul Fibrinolysis , vol.2 , pp. 293-301
    • Lavergne, J.M.1    Laurian, Y.2    Dudilleux, A.3
  • 89
    • 0026430494 scopus 로고
    • Haemophilia management: the application of DNA analysis for prenatal diagnosis
    • Van de Water NS, Ockelford PA, Berry EW, Browett PJ. Haemophilia management: the application of DNA analysis for prenatal diagnosis. N Z Med J 1991; 104: 443-446.
    • (1991) N Z Med J , vol.104 , pp. 443-446
    • Van de Water, N.S.1    Ockelford, P.A.2    Berry, E.W.3    Browett, P.J.4
  • 90
    • 0027756995 scopus 로고
    • Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques
    • Caprino D, Acquila M, Mori PG. Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques. Ann Hematol 1993; 67: 289-293.
    • (1993) Ann Hematol , vol.67 , pp. 289-293
    • Caprino, D.1    Acquila, M.2    Mori, P.G.3
  • 91
    • 0034924292 scopus 로고    scopus 로고
    • A new strategy for prenatal diagnosis in a sporadic haemophilia B family
    • Acquila M, Bottini F, Valetto A, et al. A new strategy for prenatal diagnosis in a sporadic haemophilia B family. Hemophilia 2001; 7: 416-418.
    • (2001) Hemophilia , vol.7 , pp. 416-418
    • Acquila, M.1    Bottini, F.2    Valetto, A.3
  • 92
    • 0026033622 scopus 로고
    • Prenatal diagnosis of haemophilia B by the use of polymerase chain reaction and direct sequencing
    • Ludwig M, Brackmann HH, Olek K. Prenatal diagnosis of haemophilia B by the use of polymerase chain reaction and direct sequencing. Klin Wochenschr 1991; 69: 196-200.
    • (1991) Klin Wochenschr , vol.69 , pp. 196-200
    • Ludwig, M.1    Brackmann, H.H.2    Olek, K.3
  • 93
    • 0026620631 scopus 로고
    • Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
    • Ljung R, Green P, Sjorin E, et al. Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion. Eur J Hematol 1992; 49: 215-218.
    • (1992) Eur J Hematol , vol.49 , pp. 215-218
    • Ljung, R.1    Green, P.2    Sjorin, E.3
  • 94
    • 0026481247 scopus 로고
    • Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesion
    • Schwartz M, Cooper DN, Millar DS, et al. Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesion. Prenat Diagn 1992; 12: 861-866.
    • (1992) Prenat Diagn , vol.12 , pp. 861-866
    • Schwartz, M.1    Cooper, D.N.2    Millar, D.S.3
  • 95
    • 35549003120 scopus 로고    scopus 로고
    • Prenatal diagnosis of haemophilia A by using intron 1 inversion detection
    • Salviato R, Belvini D, Zanotto D, et al. Prenatal diagnosis of haemophilia A by using intron 1 inversion detection. Hemophilia 2007; 13: 772-774.
    • (2007) Hemophilia , vol.13 , pp. 772-774
    • Salviato, R.1    Belvini, D.2    Zanotto, D.3
  • 96
    • 0042133295 scopus 로고    scopus 로고
    • Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism -Indian experience
    • Chowdhury MR, Tiwari M, Kabra M, Menon PS. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism -Indian experience. Ann Hematol 2003; 82: 427-430.
    • (2003) Ann Hematol , vol.82 , pp. 427-430
    • Chowdhury, M.R.1    Tiwari, M.2    Kabra, M.3    Menon, P.S.4
  • 97
    • 0035293431 scopus 로고    scopus 로고
    • Carrier detection and prenatal diagnosis in families with haemophilia
    • Shetty S, Ghosh K, Bhide A, Mohanty D. Carrier detection and prenatal diagnosis in families with haemophilia. Natl Med J India 2001; 14: 81-83.
    • (2001) Natl Med J India , vol.14 , pp. 81-83
    • Shetty, S.1    Ghosh, K.2    Bhide, A.3    Mohanty, D.4
  • 98
    • 21244502504 scopus 로고    scopus 로고
    • Cord blood analysis for prenatal diagnosis of thalassemia major and hemophilia A
    • Panigrahi I, Ahmed RP, Kannan M, et al. Cord blood analysis for prenatal diagnosis of thalassemia major and hemophilia A. Indian Pediatr 2005; 42: 577-581.
    • (2005) Indian Pediatr , vol.42 , pp. 577-581
    • Panigrahi, I.1    Ahmed, R.P.2    Kannan, M.3
  • 99
    • 1242309331 scopus 로고    scopus 로고
    • Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements
    • Shetty S, Ghosh K, Mohanty D. Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements. J Assoc Physicians India 2003; 51: 916-918.
    • (2003) J Assoc Physicians India , vol.51 , pp. 916-918
    • Shetty, S.1    Ghosh, K.2    Mohanty, D.3
  • 100
    • 33846903378 scopus 로고    scopus 로고
    • Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
    • Shetty S, Ghosh K. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders. Hemophilia 2007; 13: 172-177.
    • (2007) Hemophilia , vol.13 , pp. 172-177
    • Shetty, S.1    Ghosh, K.2
  • 101
    • 33645000458 scopus 로고    scopus 로고
    • Non-invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia
    • Chi C, Hyett JA, Finning KM, et al. Non-invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia. Br J Obstet Gynaecol 2006; 113: 239-242.
    • (2006) Br J Obstet Gynaecol , vol.113 , pp. 239-242
    • Chi, C.1    Hyett, J.A.2    Finning, K.M.3
  • 102
    • 0037046654 scopus 로고    scopus 로고
    • New strategy for prenatal diagnosis of X-linked disorders
    • Costa JM, Benachi A, Gautier E. New strategy for prenatal diagnosis of X-linked disorders. N Engl J Med 2002; 346: 1502.
    • (2002) N Engl J Med , vol.346 , pp. 1502
    • Costa, J.M.1    Benachi, A.2    Gautier, E.3
  • 103
    • 0036796156 scopus 로고    scopus 로고
    • Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases
    • Mazza V, Falcinelli C, Percesepe A, et al. Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases. Prenat Diagn 2002; 22: 919-924.
    • (2002) Prenat Diagn , vol.22 , pp. 919-924
    • Mazza, V.1    Falcinelli, C.2    Percesepe, A.3
  • 104
    • 26844522504 scopus 로고    scopus 로고
    • Prenatal diagnosis of von Willebrand disease in a family
    • Trasi S, Mohanty D, Shetty S, Ghosh K. Prenatal diagnosis of von Willebrand disease in a family. Natl Med J India 2005; 18: 187-188.
    • (2005) Natl Med J India , vol.18 , pp. 187-188
    • Trasi, S.1    Mohanty, D.2    Shetty, S.3    Ghosh, K.4
  • 105
    • 0018772130 scopus 로고
    • Prenatal evaluation of fetus at risk for severe von Willebrand's disease
    • Hoyer LW, Lindsten J, Blomback M, et al. Prenatal evaluation of fetus at risk for severe von Willebrand's disease. Lancet 1979; 2: 191-192.
    • (1979) Lancet , vol.2 , pp. 191-192
    • Hoyer, L.W.1    Lindsten, J.2    Blomback, M.3
  • 106
    • 0018734476 scopus 로고
    • Prenatal diagnosis of severe von Willebrand's disease
    • Rodeck CH, Mibashan RS, Peake IR, Bloom AL. Prenatal diagnosis of severe von Willebrand's disease. Lancet 1979; 2: 637-638.
    • (1979) Lancet , vol.2 , pp. 637-638
    • Rodeck, C.H.1    Mibashan, R.S.2    Peake, I.R.3    Bloom, A.L.4
  • 107
    • 0025278638 scopus 로고
    • Prenatal diagnosis in type IIA von Willebrand disease
    • Rothschild C, Forestier F, Daffos F, et al. Prenatal diagnosis in type IIA von Willebrand disease. Nouv Rev Fr Hematol 1990; 32: 125-127.
    • (1990) Nouv Rev Fr Hematol , vol.32 , pp. 125-127
    • Rothschild, C.1    Forestier, F.2    Daffos, F.3
  • 108
    • 0025183086 scopus 로고
    • Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene
    • Peake IR, Bowen D, Bignell P, et al. Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene. Blood 1990; 76: 555-561.
    • (1990) Blood , vol.76 , pp. 555-561
    • Peake, I.R.1    Bowen, D.2    Bignell, P.3
  • 109
    • 4844229372 scopus 로고    scopus 로고
    • The rare coagulation disorders -review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation
    • Bolton-Maggs PH, Perry DJ, Chalmers EA, et al. The rare coagulation disorders -review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004; 10: 593-628.
    • (2004) Haemophilia , vol.10 , pp. 593-628
    • Bolton-Maggs, P.H.1    Perry, D.J.2    Chalmers, E.A.3
  • 110
    • 33646138963 scopus 로고    scopus 로고
    • Genetic diagnosis of haemophilia and other inherited bleeding disorders
    • Peyvandi F, Jayandharan G, Chandy M, et al. Genetic diagnosis of haemophilia and other inherited bleeding disorders. Hemophilia 2006; 12 (Suppl 3): 82-89.
    • (2006) Hemophilia , vol.12 , Issue.SUPPL. 3 , pp. 82-89
    • Peyvandi, F.1    Jayandharan, G.2    Chandy, M.3
  • 111
    • 0026579362 scopus 로고
    • Prenatal exclusion of severe factor VII deficiency by DNA sequencing
    • Millar DS, Cooper DN, Kakkar VV, et al. Prenatal exclusion of severe factor VII deficiency by DNA sequencing. Lancet 1992; 339: 1359.
    • (1992) Lancet , vol.339 , pp. 1359
    • Millar, D.S.1    Cooper, D.N.2    Kakkar, V.V.3
  • 112
    • 0032147133 scopus 로고    scopus 로고
    • Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency
    • McVey JH, Boswell EJ, Takamiya O, et al. Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency. Blood 1998; 92: 920-926.
    • (1998) Blood , vol.92 , pp. 920-926
    • McVey, J.H.1    Boswell, E.J.2    Takamiya, O.3
  • 113
    • 0035134814 scopus 로고    scopus 로고
    • Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis
    • Giansily-Blaizot M, Aguilar-Martinez P, Mazurier C, et al. Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis. Br J Haematol 2001; 112: 251-252.
    • (2001) Br J Haematol , vol.112 , pp. 251-252
    • Giansily-Blaizot, M.1    Aguilar-Martinez, P.2    Mazurier, C.3
  • 115
    • 0038799915 scopus 로고    scopus 로고
    • Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism
    • Camire R, Ann DR, Day GA, III, et al. Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism. Prenat Diagn 2003; 23: 457-460.
    • (2003) Prenat Diagn , vol.23 , pp. 457-460
    • Camire, R.1    Ann, D.R.2    Day, G.A.3    III et, al.4
  • 116
    • 34248512983 scopus 로고    scopus 로고
    • Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment
    • Ingerslev J, Herlin T, Sorensen B, et al. Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment. Haemophilia 2007; 13: 334-336.
    • (2007) Haemophilia , vol.13 , pp. 334-336
    • Ingerslev, J.1    Herlin, T.2    Sorensen, B.3
  • 117
    • 0030456453 scopus 로고    scopus 로고
    • Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency
    • Kangsadalampai S, Coggan M, Caglayan SH, et al. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency. Thromb Haemost 1996; 76: 879-882.
    • (1996) Thromb Haemost , vol.76 , pp. 879-882
    • Kangsadalampai, S.1    Coggan, M.2    Caglayan, S.H.3
  • 119
    • 34247572011 scopus 로고    scopus 로고
    • Second trimester antenatal diagnosis in rare coagulation factor deficiencies
    • Mota L, Ghosh K, Shetty S. Second trimester antenatal diagnosis in rare coagulation factor deficiencies. J Pediatr Hematol Oncol 2007; 29: 137-139.
    • (2007) J Pediatr Hematol Oncol , vol.29 , pp. 137-139
    • Mota, L.1    Ghosh, K.2    Shetty, S.3
  • 120
    • 0024515059 scopus 로고
    • Biopsy of human preimplantation embryos and sexing by DNA amplification
    • Handyside AH, Pattinson JK, Penketh RJ, et al. Biopsy of human preimplantation embryos and sexing by DNA amplification. Lancet 1989; 1: 347-349.
    • (1989) Lancet , vol.1 , pp. 347-349
    • Handyside, A.H.1    Pattinson, J.K.2    Penketh, R.J.3
  • 121
    • 0025307919 scopus 로고
    • Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification
    • Handyside AH, Kontogianni EH, Hardy K, Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990; 344: 768-770.
    • (1990) Nature , vol.344 , pp. 768-770
    • Handyside, A.H.1    Kontogianni, E.H.2    Hardy, K.3    Winston, R.M.4
  • 123
    • 33846481340 scopus 로고    scopus 로고
    • ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004
    • Sermon KD, Michiels A, Harton G, et al. ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004. Hum Reprod 2007; 22: 323-336.
    • (2007) Hum Reprod , vol.22 , pp. 323-336
    • Sermon, K.D.1    Michiels, A.2    Harton, G.3
  • 124
    • 0031404915 scopus 로고    scopus 로고
    • Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body
    • Verlinsky Y, Rechitsky S, Cieslak J, et al. Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body. Biochem Mol Med 1997; 62: 182-187.
    • (1997) Biochem Mol Med , vol.62 , pp. 182-187
    • Verlinsky, Y.1    Rechitsky, S.2    Cieslak, J.3
  • 125
    • 0031777523 scopus 로고    scopus 로고
    • Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis
    • Strom CM, Ginsberg N, Rechitsky S, et al. Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis. Am J Obstet Gynecol 1998; 178: 1298-1306.
    • (1998) Am J Obstet Gynecol , vol.178 , pp. 1298-1306
    • Strom, C.M.1    Ginsberg, N.2    Rechitsky, S.3
  • 126
    • 14844293141 scopus 로고    scopus 로고
    • Polar body diagnosis for hemophilia A using multiplex PCR for linked polymorphic markers
    • Tomi D, Griesinger G, Schultze-Mosgau A, et al. Polar body diagnosis for hemophilia A using multiplex PCR for linked polymorphic markers. J Histochem Cytochem 2005; 53: 277-280.
    • (2005) J Histochem Cytochem , vol.53 , pp. 277-280
    • Tomi, D.1    Griesinger, G.2    Schultze-Mosgau, A.3
  • 127
    • 0025180503 scopus 로고
    • Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage
    • Hardy K, Martin KL, Leese HJ, et al. Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage. Hum Reprod 1990; 5: 708-714.
    • (1990) Hum Reprod , vol.5 , pp. 708-714
    • Hardy, K.1    Martin, K.L.2    Leese, H.J.3
  • 128
    • 0034512073 scopus 로고    scopus 로고
    • Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to preimplantation genetic diagnosis
    • Van de Velde H, De Vos A, Sermon K, et al. Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to preimplantation genetic diagnosis. Prenat Diagn 2000; 20: 1030-1037.
    • (2000) Prenat Diagn , vol.20 , pp. 1030-1037
    • Van de Velde, H.1    De Vos, A.2    Sermon, K.3
  • 129
    • 0032402363 scopus 로고    scopus 로고
    • Factors affecting the success of human blastocyst development and pregnancy following in vitro fertilization and embryo transfer
    • Jones GM, Trounson AO, Lolatgis N, Wood C. Factors affecting the success of human blastocyst development and pregnancy following in vitro fertilization and embryo transfer. Fertil Steril 1998; 70: 1022-1029.
    • (1998) Fertil Steril , vol.70 , pp. 1022-1029
    • Jones, G.M.1    Trounson, A.O.2    Lolatgis, N.3    Wood, C.4
  • 130
    • 0033214128 scopus 로고    scopus 로고
    • Blastocyst culture and transfer: analysis of results and parameters affecting outcome in two in vitro fertilization programs
    • Schoolcraft WB, Gardner DK, Lane M, et al. Blastocyst culture and transfer: analysis of results and parameters affecting outcome in two in vitro fertilization programs. Fertil Steril 1999; 72: 604-609.
    • (1999) Fertil Steril , vol.72 , pp. 604-609
    • Schoolcraft, W.B.1    Gardner, D.K.2    Lane, M.3
  • 132
    • 0038825355 scopus 로고    scopus 로고
    • The minisequencing method: an alternative strategy for preimplantation genetic diagnosis of single gene disorders
    • Fiorentino F, Magli MC, Podini D, et al. The minisequencing method: an alternative strategy for preimplantation genetic diagnosis of single gene disorders. Mol Hum Reprod 2003; 9: 399-410.
    • (2003) Mol Hum Reprod , vol.9 , pp. 399-410
    • Fiorentino, F.1    Magli, M.C.2    Podini, D.3
  • 133
    • 33645552865 scopus 로고    scopus 로고
    • Live birth following the first mutation specific preimplantation genetic diagnosis for haemophilia A
    • Michaelides K, Tuddenham EG, Turner C, et al. Live birth following the first mutation specific preimplantation genetic diagnosis for haemophilia A. Thromb Hemost 2006; 95: 373-379.
    • (2006) Thromb Hemost , vol.95 , pp. 373-379
    • Michaelides, K.1    Tuddenham, E.G.2    Turner, C.3
  • 134
    • 1142263131 scopus 로고    scopus 로고
    • Single cell coamplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, Xlinked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28
    • Gigarel N, Frydman N, Burlet P, et al. Single cell coamplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, Xlinked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28. Hum Genet 2004; 114: 298-305.
    • (2004) Hum Genet , vol.114 , pp. 298-305
    • Gigarel, N.1    Frydman, N.2    Burlet, P.3
  • 135
    • 84889624649 scopus 로고    scopus 로고
    • Department of Health, Preimplantation genetic diagnosis (PGD): guiding principles for commissioners of NHS services, Department of Health: London
    • Department of Health. Preimplantation genetic diagnosis (PGD): guiding principles for commissioners of NHS services. Department of Health: London 2002.
    • (2002)
  • 136
    • 19944432386 scopus 로고    scopus 로고
    • ESHRE PGD Consortium "Best practice guidelines for clinical preimplantation genetic diagnosis (PGD and preimplantation genetic screening (PGS)"
    • Thornhill AR, deDie-Smulders CE, Geraedts JP, et al. ESHRE PGD Consortium "Best practice guidelines for clinical preimplantation genetic diagnosis (PGD and preimplantation genetic screening (PGS)". Hum Reprod 2005; 20: 35-48.
    • (2005) Hum Reprod , vol.20 , pp. 35-48
    • Thornhill, A.R.1    deDie-Smulders, C.E.2    Geraedts, J.P.3
  • 137
    • 0029030756 scopus 로고
    • DNA-based Xenriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease
    • Levinson G, Keyvanfar K, Wu JC, et al. DNA-based Xenriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease. Hum Reprod 1995; 10: 979-982.
    • (1995) Hum Reprod , vol.10 , pp. 979-982
    • Levinson, G.1    Keyvanfar, K.2    Wu, J.C.3
  • 138
    • 0031659860 scopus 로고    scopus 로고
    • Births of normal daughters after MicroSort sperm separation and intrauterine insemination, in-vitro fertilization, or intracytoplasmic sperm injection
    • Fugger EF, Black SH, Keyvanfar K, Schulman JD. Births of normal daughters after MicroSort sperm separation and intrauterine insemination, in-vitro fertilization, or intracytoplasmic sperm injection. Hum Reprod 1998; 13: 2367-2370.
    • (1998) Hum Reprod , vol.13 , pp. 2367-2370
    • Fugger, E.F.1    Black, S.H.2    Keyvanfar, K.3    Schulman, J.D.4
  • 139
    • 0017113805 scopus 로고
    • A difference in dry mass between the heads of X- and Y-bearing human spermatozoa
    • Sumner AT, Robinson JA. A difference in dry mass between the heads of X- and Y-bearing human spermatozoa. J Reprod Fertil 1976; 48: 9-15.
    • (1976) J Reprod Fertil , vol.48 , pp. 9-15
    • Sumner, A.T.1    Robinson, J.A.2
  • 140
    • 0030630165 scopus 로고    scopus 로고
    • Size differences between human X and Y spermatozoa and prefertilization diagnosis
    • Cui KH. Size differences between human X and Y spermatozoa and prefertilization diagnosis. Mol Hum Reprod 1997; 3: 61-67.
    • (1997) Mol Hum Reprod , vol.3 , pp. 61-67
    • Cui, K.H.1
  • 141
    • 0027380114 scopus 로고
    • Gender preselection in humans?. Flow cytometric separation of X and Y spermatozoa for the prevention of X-linked diseases
    • Johnson LA, Welch GR, Keyvanfar K, et al. Gender preselection in humans?. Flow cytometric separation of X and Y spermatozoa for the prevention of X-linked diseases. Hum Reprod 1993; 8: 1733-1739.
    • (1993) Hum Reprod , vol.8 , pp. 1733-1739
    • Johnson, L.A.1    Welch, G.R.2    Keyvanfar, K.3
  • 142
    • 0028831024 scopus 로고
    • Fluorescent in situ hybridization evaluation of human Y-bearing spermatozoa separated by albumin density gradients
    • Claassens OE, Oosthuizen CJ, Brusnicky J, et al. Fluorescent in situ hybridization evaluation of human Y-bearing spermatozoa separated by albumin density gradients. Fertil Steril 1995; 63: 417-418.
    • (1995) Fertil Steril , vol.63 , pp. 417-418
    • Claassens, O.E.1    Oosthuizen, C.J.2    Brusnicky, J.3
  • 143
    • 0028205592 scopus 로고
    • Assessment of the separation of X- and Y-bearing sperm on albumin gradients using double-label fluorescence in situ hybridization
    • Wang HX, Flaherty SP, Swann NJ, Matthews CD. Assessment of the separation of X- and Y-bearing sperm on albumin gradients using double-label fluorescence in situ hybridization. Fertil Steril 1994; 61: 720-726.
    • (1994) Fertil Steril , vol.61 , pp. 720-726
    • Wang, H.X.1    Flaherty, S.P.2    Swann, N.J.3    Matthews, C.D.4
  • 144
    • 0030959081 scopus 로고    scopus 로고
    • Albumin gradients do not enrich Y-bearing human spermatozoa
    • Flaherty SP, Michalowska J, Swann NJ, et al. Albumin gradients do not enrich Y-bearing human spermatozoa. Hum Reprod 1997; 12: 938-942.
    • (1997) Hum Reprod , vol.12 , pp. 938-942
    • Flaherty, S.P.1    Michalowska, J.2    Swann, N.J.3
  • 146
    • 0027402915 scopus 로고
    • The sex ratio of normal and manipulated human sperm quantitated by the polymerase chain reaction
    • Lobel SM, Pomponio RJ, Mutter GL. The sex ratio of normal and manipulated human sperm quantitated by the polymerase chain reaction. Fertil Steril 1993; 59: 387-392.
    • (1993) Fertil Steril , vol.59 , pp. 387-392
    • Lobel, S.M.1    Pomponio, R.J.2    Mutter, G.L.3
  • 147
    • 0027377483 scopus 로고
    • Sephadex filtration and human serum albumin gradients do not select spermatozoa by sex chromosome: a fluorescent in-situ hybridization study
    • Vidal F, Moragas M, Catala V, et al. Sephadex filtration and human serum albumin gradients do not select spermatozoa by sex chromosome: a fluorescent in-situ hybridization study. Hum Reprod 1993; 8: 1740-1743.
    • (1993) Hum Reprod , vol.8 , pp. 1740-1743
    • Vidal, F.1    Moragas, M.2    Catala, V.3
  • 148
    • 0028282415 scopus 로고
    • Discontinuous Percoll gradients enrich X-bearing human spermatozoa: a study using double-label fluorescence in-situ hybridization
    • Wang HX, Flaherty SP, Swann NJ, Matthews CD. Discontinuous Percoll gradients enrich X-bearing human spermatozoa: a study using double-label fluorescence in-situ hybridization. Hum Reprod 1994; 9: 1265-1270.
    • (1994) Hum Reprod , vol.9 , pp. 1265-1270
    • Wang, H.X.1    Flaherty, S.P.2    Swann, N.J.3    Matthews, C.D.4
  • 149
    • 0031766686 scopus 로고    scopus 로고
    • Separating X-bearing human spermatozoa through a discontinuous Percoll density gradient proved to be inefficient by double-label fluorescent in situ hybridization
    • Lin SP, Lee RK, Tsai YJ, et al. Separating X-bearing human spermatozoa through a discontinuous Percoll density gradient proved to be inefficient by double-label fluorescent in situ hybridization. J Assist Reprod Genet 1998; 15: 565-569.
    • (1998) J Assist Reprod Genet , vol.15 , pp. 565-569
    • Lin, S.P.1    Lee, R.K.2    Tsai, Y.J.3
  • 150
    • 0031887994 scopus 로고    scopus 로고
    • Efficiency of Micro- Sort flow cytometry for producing sperm populations enriched in X- or Y-chromosome haplotypes: a blind trial assessed by double and triple colour fluorescent insitu hybridization
    • Vidal F, Fugger EF, Blanco J, et al. Efficiency of Micro- Sort flow cytometry for producing sperm populations enriched in X- or Y-chromosome haplotypes: a blind trial assessed by double and triple colour fluorescent insitu hybridization. Hum Reprod 1998; 13: 308-312.
    • (1998) Hum Reprod , vol.13 , pp. 308-312
    • Vidal, F.1    Fugger, E.F.2    Blanco, J.3
  • 151
    • 0033397108 scopus 로고    scopus 로고
    • Clinical experience with flow cytometric separation of human X- and Y-chromosome bearing sperm
    • Fugger EF. Clinical experience with flow cytometric separation of human X- and Y-chromosome bearing sperm. Theriogenology 1999; 52: 1435-1440.
    • (1999) Theriogenology , vol.52 , pp. 1435-1440
    • Fugger, E.F.1
  • 155
    • 0034734711 scopus 로고    scopus 로고
    • Prenatal DNA diagnosis of a single-gene disorder from maternal plasma
    • Saito H, Sekizawa A, Morimoto T, et al. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Lancet 2000; 356: 1170.
    • (2000) Lancet , vol.356 , pp. 1170
    • Saito, H.1    Sekizawa, A.2    Morimoto, T.3
  • 156
    • 9644273981 scopus 로고    scopus 로고
    • Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma -case report
    • Li Y, Holzgreve W, Page-Christiaens GC, et al. Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma -case report. Prenat Diagn 2004; 24: 896-898.
    • (2004) Prenat Diagn , vol.24 , pp. 896-898
    • Li, Y.1    Holzgreve, W.2    Page-Christiaens, G.C.3
  • 157
    • 0033968645 scopus 로고    scopus 로고
    • Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
    • Amicucci P, Gennarelli M, Novelli G, Dallapiccola B. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Clin Chem 2000; 46: 301-302.
    • (2000) Clin Chem , vol.46 , pp. 301-302
    • Amicucci, P.1    Gennarelli, M.2    Novelli, G.3    Dallapiccola, B.4
  • 158
    • 13844269123 scopus 로고    scopus 로고
    • Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma
    • Li Y, Di Naro E, Vitucci A, et al. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. JAMA 2005; 293: 843-849.
    • (2005) JAMA , vol.293 , pp. 843-849
    • Li, Y.1    Di Naro, E.2    Vitucci, A.3
  • 159
    • 0037190608 scopus 로고    scopus 로고
    • Prenatal exclusion of beta thalassaemia major by examination of maternal plasma
    • Chiu RW, Lau TK, Leung TN, et al. Prenatal exclusion of beta thalassaemia major by examination of maternal plasma. Lancet 2002; 360: 998-1000.
    • (2002) Lancet , vol.360 , pp. 998-1000
    • Chiu, R.W.1    Lau, T.K.2    Leung, T.N.3
  • 160
    • 0037406282 scopus 로고    scopus 로고
    • Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes
    • Vrettou C, Traeger-Synodinos J, Tzetis M, et al. Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes. Clin Chem 2003; 49: 769-776.
    • (2003) Clin Chem , vol.49 , pp. 769-776
    • Vrettou, C.1    Traeger-Synodinos, J.2    Tzetis, M.3
  • 161
    • 1842503944 scopus 로고    scopus 로고
    • Improvement in sensitivity of allele-specific PCR facilitates reliable noninvasive prenatal detection of cystic fibrosis
    • Nasis O, Thompson S, Hong T, et al. Improvement in sensitivity of allele-specific PCR facilitates reliable noninvasive prenatal detection of cystic fibrosis. Clin Chem 2004; 50: 694-701.
    • (2004) Clin Chem , vol.50 , pp. 694-701
    • Nasis, O.1    Thompson, S.2    Hong, T.3
  • 162
    • 0036797932 scopus 로고    scopus 로고
    • Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma
    • Gonzalez-Gonzalez MC, Garcia-Hoyos M, Trujillo MJ, et al. Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma. Prenat Diagn 2002; 22: 946-948.
    • (2002) Prenat Diagn , vol.22 , pp. 946-948
    • Gonzalez-Gonzalez, M.C.1    Garcia-Hoyos, M.2    Trujillo, M.J.3
  • 163
    • 33646023698 scopus 로고    scopus 로고
    • Recent developments in fetal nucleic acids in maternal plasma: implications to noninvasive prenatal fetal blood group genotyping
    • Lo YM. Recent developments in fetal nucleic acids in maternal plasma: implications to noninvasive prenatal fetal blood group genotyping. Transfus Clin Biol 2006; 13: 50-52.
    • (2006) Transfus Clin Biol , vol.13 , pp. 50-52
    • Lo, Y.M.1
  • 165
    • 0027250859 scopus 로고
    • Presence of fetal cells in maternal circulation after delivery
    • Hsieh TT, Pao CC, Hor JJ, Kao SM. Presence of fetal cells in maternal circulation after delivery. Hum Genet 1993; 92: 204-205.
    • (1993) Hum Genet , vol.92 , pp. 204-205
    • Hsieh, T.T.1    Pao, C.C.2    Hor, J.J.3    Kao, S.M.4
  • 166
    • 0027999953 scopus 로고
    • Presence of cells of fetal origin in maternal circulation of pregnant women
    • Liou JD, Hsieh TT, Pao CC. Presence of cells of fetal origin in maternal circulation of pregnant women. Ann NY Acad Sci 1994; 731: 237-241.
    • (1994) Ann NY Acad Sci , vol.731 , pp. 237-241
    • Liou, J.D.1    Hsieh, T.T.2    Pao, C.C.3
  • 167
    • 0023732315 scopus 로고
    • Circulating "trophoblast" cells in pregnancy have maternal genetic markers
    • Bertero MT, Camaschella C, Serra A, et al. Circulating "trophoblast" cells in pregnancy have maternal genetic markers. Prenat Diagn 1988; 8: 585-590.
    • (1988) Prenat Diagn , vol.8 , pp. 585-590
    • Bertero, M.T.1    Camaschella, C.2    Serra, A.3
  • 168
    • 0023791807 scopus 로고
    • Analysis of peripheral maternal blood samples for the presence of placenta-derived cells using Y-specific probes and McAb H315
    • Covone AE, Kozma R, Johnson PM, et al. Analysis of peripheral maternal blood samples for the presence of placenta-derived cells using Y-specific probes and McAb H315. Prenat Diagn 1988; 8: 591-607.
    • (1988) Prenat Diagn , vol.8 , pp. 591-607
    • Covone, A.E.1    Kozma, R.2    Johnson, P.M.3
  • 169
    • 0028295383 scopus 로고
    • Fetal cells in maternal circulation throughout gestation
    • Ganshirt D, Garritsen H, Miny P, Holzgreve W. Fetal cells in maternal circulation throughout gestation. Lancet 1994; 343: 1038-1039.
    • (1994) Lancet , vol.343 , pp. 1038-1039
    • Ganshirt, D.1    Garritsen, H.2    Miny, P.3    Holzgreve, W.4
  • 170
    • 0014054213 scopus 로고
    • Life-span of the fetal red blood cell
    • Pearson HA. Life-span of the fetal red blood cell. J Pediatr 1967; 70: 166-171.
    • (1967) J Pediatr , vol.70 , pp. 166-171
    • Pearson, H.A.1
  • 171
    • 0025364769 scopus 로고
    • Isolation of fetal DNA from nucleated erythrocytes in maternal blood
    • Bianchi DW, Flint AF, Pizzimenti MF, et al. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc Natl Acad Sci USA 1990; 87: 3279-3283.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 3279-3283
    • Bianchi, D.W.1    Flint, A.F.2    Pizzimenti, M.F.3
  • 173
    • 0028870055 scopus 로고
    • Mid-trimester fetal sex determination from maternal peripheral blood by fluorescence in situ hybridization without enrichment of fetal cells
    • Hamada H, Arinami T, Sohda S, et al. Mid-trimester fetal sex determination from maternal peripheral blood by fluorescence in situ hybridization without enrichment of fetal cells. Prenat Diagn 1995; 15: 78-81.
    • (1995) Prenat Diagn , vol.15 , pp. 78-81
    • Hamada, H.1    Arinami, T.2    Sohda, S.3
  • 174
    • 0029041181 scopus 로고
    • Maternal origin of nucleated erythrocytes in peripheral venous blood of pregnant women
    • Slunga-Tallberg A, el Rifai W, Keinanen M, et al. Maternal origin of nucleated erythrocytes in peripheral venous blood of pregnant women. Hum Genet 1995; 96: 53-57.
    • (1995) Hum Genet , vol.96 , pp. 53-57
    • Slunga-Tallberg, A.1    El Rifai, W.2    Keinanen, M.3
  • 175
    • 0029945828 scopus 로고    scopus 로고
    • Maternal origin of transferrin receptor positive cells in venous blood of pregnant women
    • Slunga-Tallberg A, el Rifai W, Keinanen M, et al. Maternal origin of transferrin receptor positive cells in venous blood of pregnant women. Clin Genet 1996; 49: 196-199.
    • (1996) Clin Genet , vol.49 , pp. 196-199
    • Slunga-Tallberg, A.1    El Rifai, W.2    Keinanen, M.3
  • 176
    • 0034004651 scopus 로고    scopus 로고
    • Reproductive choices of women in families with haemophilia
    • Kadir RA, Sabin CA, Goldman E, et al. Reproductive choices of women in families with haemophilia. Hemophilia 2000; 6: 33-40.
    • (2000) Hemophilia , vol.6 , pp. 33-40
    • Kadir, R.A.1    Sabin, C.A.2    Goldman, E.3
  • 177
    • 0021917950 scopus 로고
    • Decision making: whether or not to have prenatal diagnosis and abortion for Xlinked conditions
    • Beeson D, Golbus MS. Decision making: whether or not to have prenatal diagnosis and abortion for Xlinked conditions. Am J Med Genet 1985; 20: 107-114.
    • (1985) Am J Med Genet , vol.20 , pp. 107-114
    • Beeson, D.1    Golbus, M.S.2
  • 178
    • 0034004651 scopus 로고    scopus 로고
    • Reproductive choices of women in families with haemophilia
    • Kadir RA, Sabin CA, Goldman E, et al. Reproductive choices of women in families with haemophilia. Hemophilia 2000; 6: 33-40.
    • (2000) Hemophilia , vol.6 , pp. 33-40
    • Kadir, R.A.1    Sabin, C.A.2    Goldman, E.3
  • 179
    • 0023696744 scopus 로고
    • Assessment of reproductive risks and intentions by mothers of children with hemophilia
    • Kraus EM, Brettler DB. Assessment of reproductive risks and intentions by mothers of children with hemophilia. Am J Med Genet 1988; 31: 259-267.
    • (1988) Am J Med Genet , vol.31 , pp. 259-267
    • Kraus, E.M.1    Brettler, D.B.2
  • 180
    • 0032870816 scopus 로고    scopus 로고
    • Reproductive choices of haemophilia carriers
    • Tedgard U, Ljung R, McNeil TF. Reproductive choices of haemophilia carriers. Br J Hematol 1999; 106: 421-426.
    • (1999) Br J Hematol , vol.106 , pp. 421-426
    • Tedgard, U.1    Ljung, R.2    McNeil, T.F.3
  • 181
    • 0025063290 scopus 로고
    • Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers
    • Varekamp I, Suurmeijer TP, Brocker-Vriends AH, et al. Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers. Am J Med Genet 1990; 37: 147-154.
    • (1990) Am J Med Genet , vol.37 , pp. 147-154
    • Varekamp, I.1    Suurmeijer, T.P.2    Brocker-Vriends, A.H.3
  • 182
    • 0021166063 scopus 로고
    • The consumers' views of genetic counseling of hemophilia
    • Markova I, Forbes CD, Inwood M. The consumers' views of genetic counseling of hemophilia. Am J Med Genet 1984; 17: 741-752.
    • (1984) Am J Med Genet , vol.17 , pp. 741-752
    • Markova, I.1    Forbes, C.D.2    Inwood, M.3
  • 183
    • 0021076703 scopus 로고
    • Reproduction in hemophilia
    • Francis RB, Jr., Kasper CK. Reproduction in hemophilia. JAMA 1983; 250: 3192-3195.
    • (1983) JAMA , vol.250 , pp. 3192-3195
    • Francis, Jr.R.B.1    Kasper, C.K.2
  • 185
    • 37749037035 scopus 로고    scopus 로고
    • Pregnancy in carriers of haemophilia
    • Chi C, Lee CA, Shiltagh N, et al. Pregnancy in carriers of haemophilia. Hemophilia 2008; 14: 56-64.
    • (2008) Hemophilia , vol.14 , pp. 56-64
    • Chi, C.1    Lee, C.A.2    Shiltagh, N.3
  • 186
    • 0021832891 scopus 로고
    • Prenatal diagnosis of classic hemophilia (hemophilia A by immunoradiometric assays
    • Hoyer LW, Carta CA, Golbus MS, et al. Prenatal diagnosis of classic hemophilia (hemophilia A by immunoradiometric assays. Blood 1985; 65: 1312-1317.
    • (1985) Blood , vol.65 , pp. 1312-1317
    • Hoyer, L.W.1    Carta, C.A.2    Golbus, M.S.3
  • 187
    • 0344450767 scopus 로고    scopus 로고
    • How do carriers of hemophilia and their spouses experience prenatal diagnosis by chorionic villus sampling?
    • Tedgard U, Ljung R, McNeil TF. How do carriers of hemophilia and their spouses experience prenatal diagnosis by chorionic villus sampling?. Clin Genet 1999; 55: 26-33.
    • (1999) Clin Genet , vol.55 , pp. 26-33
    • Tedgard, U.1    Ljung, R.2    McNeil, T.F.3
  • 188
    • 4043096285 scopus 로고    scopus 로고
    • Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy
    • Karimi M, Peyvandi F, Siboni S, et al. Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy. Hemophilia 2004; 10: 367-369.
    • (2004) Hemophilia , vol.10 , pp. 367-369
    • Karimi, M.1    Peyvandi, F.2    Siboni, S.3
  • 189
    • 0142156664 scopus 로고    scopus 로고
    • Knowledge and attitudes towards haemophilia: the family side and role of haemophilia societies
    • Pandey GS, Panigrahi I, Phadke SR, Mittal B. Knowledge and attitudes towards haemophilia: the family side and role of haemophilia societies. Community Genet 2003; 6: 120-122.
    • (2003) Community Genet , vol.6 , pp. 120-122
    • Pandey, G.S.1    Panigrahi, I.2    Phadke, S.R.3    Mittal, B.4
  • 190
    • 27844606354 scopus 로고    scopus 로고
    • Carrier detection and prenatal diagnosis of hemophilia in developing countries
    • Peyvandi F. Carrier detection and prenatal diagnosis of hemophilia in developing countries. Semin Thromb Hemost 2005; 31: 544-554.
    • (2005) Semin Thromb Hemost , vol.31 , pp. 544-554
    • Peyvandi, F.1
  • 191
    • 0036210959 scopus 로고    scopus 로고
    • Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges
    • Ghosh K, Shetty S, Pawar A, Mohanty D. Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges. Hemophilia 2002; 8: 51-55.
    • (2002) Hemophilia , vol.8 , pp. 51-55
    • Ghosh, K.1    Shetty, S.2    Pawar, A.3    Mohanty, D.4
  • 192
    • 0025309065 scopus 로고
    • Prenatal diagnosis for psychological reasons: comparison with other indications, advanced maternal age and known genetic risk
    • Sjogren B, Uddenberg N. Prenatal diagnosis for psychological reasons: comparison with other indications, advanced maternal age and known genetic risk. Prenat Diagn 1990; 10: 111-120.
    • (1990) Prenat Diagn , vol.10 , pp. 111-120
    • Sjogren, B.1    Uddenberg, N.2
  • 193
    • 0023873215 scopus 로고
    • Psychological aspects of amniocentesis: anxiety feelings in three different risk groups
    • Evers-Kiebooms G, Swerts A, van den Berge H. Psychological aspects of amniocentesis: anxiety feelings in three different risk groups. Clin Genet 1988; 33: 196-206.
    • (1988) Clin Genet , vol.33 , pp. 196-206
    • Evers-Kiebooms, G.1    Swerts, A.2    van den Berge, H.3
  • 194
    • 0016590394 scopus 로고
    • Amniocentesis: its impact on mothers and infants A 1-year follow-up study
    • Robinson J, Tennes K, Robinson A. Amniocentesis: its impact on mothers and infants. A 1-year follow-up study. Clin Genet 1975; 8: 97-106.
    • (1975) Clin Genet , vol.8 , pp. 97-106
    • Robinson, J.1    Tennes, K.2    Robinson, A.3
  • 195
    • 0023629645 scopus 로고
    • Emotional responses of pregnant women to chorionic villi sampling or amniocentesis
    • Spencer JW, Cox DN. Emotional responses of pregnant women to chorionic villi sampling or amniocentesis. Am J Obstet Gynecol 1987; 157: 1155-1160.
    • (1987) Am J Obstet Gynecol , vol.157 , pp. 1155-1160
    • Spencer, J.W.1    Cox, D.N.2
  • 196
    • 0023727694 scopus 로고
    • Anxiety reduction after chorionic villus sampling and genetic amniocentesis
    • Robinson GE, Garner DM, Olmsted MP, et al. Anxiety reduction after chorionic villus sampling and genetic amniocentesis. Am J Obstet Gynecol 1988; 159: 953-956.
    • (1988) Am J Obstet Gynecol , vol.159 , pp. 953-956
    • Robinson, G.E.1    Garner, D.M.2    Olmsted, M.P.3
  • 197
    • 0024397748 scopus 로고
    • Prenatal diagnosis and psychological distress: amniocentesis or chorionic villus biopsy?
    • Sjogren B, Uddenberg N. Prenatal diagnosis and psychological distress: amniocentesis or chorionic villus biopsy?. Prenat Diagn 1989; 9: 477-487.
    • (1989) Prenat Diagn , vol.9 , pp. 477-487
    • Sjogren, B.1    Uddenberg, N.2
  • 198
    • 0024790801 scopus 로고
    • A 1 and 6 month follow-up of prenatal diagnosis patients who lost pregnancies
    • Black RB. A 1 and 6 month follow-up of prenatal diagnosis patients who lost pregnancies. Prenat Diagn 1989; 9: 795-804.
    • (1989) Prenat Diagn , vol.9 , pp. 795-804
    • Black, R.B.1
  • 199
    • 0024444743 scopus 로고
    • How do carriers of hemophilia experience prenatal diagnosis (PND)?. Carriers' immediate and later reactions to amniocentesis and fetal blood sampling
    • Tedgard, Ljung R, McNeil T, et al. How do carriers of hemophilia experience prenatal diagnosis (PND)?. Carriers' immediate and later reactions to amniocentesis and fetal blood sampling. Acta Paediatr Scand 1989; 78: 692-700.
    • (1989) Acta Paediatr Scand , vol.78 , pp. 692-700
    • Tedgard Ljung, R.1    McNeil, T.2
  • 200
    • 0030902308 scopus 로고    scopus 로고
    • Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia
    • Tedgard U, Ljung R, McNeil TF, Tedgard E. Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia. Hemophilia 1997; 3: 123-130.
    • (1997) Hemophilia , vol.3 , pp. 123-130
    • Tedgard, U.1    Ljung, R.2    McNeil, T.F.3    Tedgard, E.4
  • 201
    • 0017595687 scopus 로고
    • Confirmation of the dimensional structure of the SCL-90 A study in construct validity
    • Derogatis LR, Lipman RS, Cleary PA. Confirmation of the dimensional structure of the SCL-90. A study in construct validity. J Clin Psychol 1977; 33: 981-989.
    • (1977) J Clin Psychol , vol.33 , pp. 981-989
    • Derogatis, L.R.1    Lipman, R.S.2    Cleary, P.A.3
  • 202
    • 0345189528 scopus 로고    scopus 로고
    • Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: comparison with a control group
    • Tedgard U, Ljung R, McNeil TF. Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: comparison with a control group. Prenat Diagn 1999; 19: 411-417.
    • (1999) Prenat Diagn , vol.19 , pp. 411-417
    • Tedgard, U.1    Ljung, R.2    McNeil, T.F.3
  • 203
    • 0019948521 scopus 로고
    • Current status of Swedish haemophiliacs. I. A demographic survey
    • Larsson SA, Nilsson IM, Blomback M. Current status of Swedish haemophiliacs. I. A demographic survey. Acta Med Scand 1982; 212: 195-200.
    • (1982) Acta Med Scand , vol.212 , pp. 195-200
    • Larsson, S.A.1    Nilsson, I.M.2    Blomback, M.3
  • 204
    • 84980304661 scopus 로고
    • The impact of prenatal diagnosis on the incidence of haemophilia in Sweden
    • Ljung R, Kling S, Tedgard U. The impact of prenatal diagnosis on the incidence of haemophilia in Sweden. Hemophilia 1995; 1: 190-193.
    • (1995) Hemophilia , vol.1 , pp. 190-193
    • Ljung, R.1    Kling, S.2    Tedgard, U.3
  • 205
    • 0034004651 scopus 로고    scopus 로고
    • Reproductive choices of women in families with haemophilia
    • Kadir RA, Sabin CA, Goldman E, et al. Reproductive choices of women in families with haemophilia. Hemophilia 2000; 6: 33-40.
    • (2000) Hemophilia , vol.6 , pp. 33-40
    • Kadir, R.A.1    Sabin, C.A.2    Goldman, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.