메뉴 건너뛰기




Volumn 48, Issue 3, 2009, Pages 218-224

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (II)

Author keywords

congenital malformations; prenatal diagnosis; trisomy 13; ultrasound

Indexed keywords

BRACHYCEPHALY; BRAIN MALFORMATION; CHROMOSOME ABERRATION; CLEFT PALATE; CLINICAL FEATURE; DANDY WALKER SYNDROME; DISEASE ASSOCIATION; FETUS ECHOGRAPHY; HOLOPROSENCEPHALY; HUMAN; MICROCEPHALY; MICROGNATHIA; NEURAL TUBE DEFECT; POSTERIOR FOSSA; PRENATAL DIAGNOSIS; PREVALENCE; REVIEW; SECOND TRIMESTER PREGNANCY; THIRD TRIMESTER PREGNANCY; TRISOMY 13; CHROMOSOME 13; ECHOGRAPHY; FEMALE; FETUS DISEASE; GENETICS; MULTIPLE MALFORMATION SYNDROME; PREGNANCY; TRISOMY;

EID: 73449115725     PISSN: None     EISSN: 10284559     Source Type: Journal    
DOI: 10.1016/S1028-4559(09)60293-X     Document Type: Review
Times cited : (23)

References (63)
  • 1
    • 73449130564 scopus 로고    scopus 로고
    • Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I)
    • Chen C.P. Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I). Taiwan J Obstet Gynecol 48 3 (2009) 210-217
    • (2009) Taiwan J Obstet Gynecol , vol.48 , Issue.3 , pp. 210-217
    • Chen, C.P.1
  • 2
    • 0011977665 scopus 로고
    • Holoprosencephaly as a genetic model to study normal craniofacial development
    • Muenke M. Holoprosencephaly as a genetic model to study normal craniofacial development. Semin Dev Biol 5 (1994) 293-301
    • (1994) Semin Dev Biol , vol.5 , pp. 293-301
    • Muenke, M.1
  • 3
    • 0036170640 scopus 로고    scopus 로고
    • Molecular diagnosis of a novel heterozygous 268C T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis
    • Chen C.P., Chern S.R., Du S.H., and Wang W. Molecular diagnosis of a novel heterozygous 268C T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis. Prenat Diagn 22 (2002) 5-7
    • (2002) Prenat Diagn , vol.22 , pp. 5-7
    • Chen, C.P.1    Chern, S.R.2    Du, S.H.3    Wang, W.4
  • 4
    • 16444365690 scopus 로고    scopus 로고
    • Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes
    • Chen C.P., Chen C.Y., Lin C.Y., Shaw S.W., Wang W., and Tzen C.Y. Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes. Prenat Diagn 25 (2005) 264-266
    • (2005) Prenat Diagn , vol.25 , pp. 264-266
    • Chen, C.P.1    Chen, C.Y.2    Lin, C.Y.3    Shaw, S.W.4    Wang, W.5    Tzen, C.Y.6
  • 5
    • 11144294107 scopus 로고    scopus 로고
    • Perinatal identification of caudal regression syndrome and alobar holoprosencephaly in pregnancies with poor maternal metabolic control
    • Chen C.P. Perinatal identification of caudal regression syndrome and alobar holoprosencephaly in pregnancies with poor maternal metabolic control. Genet Couns 15 (2004) 485-488
    • (2004) Genet Couns , vol.15 , pp. 485-488
    • Chen, C.P.1
  • 6
    • 17144382464 scopus 로고    scopus 로고
    • Congenital malformations associated with maternal diabetes
    • Chen C.P. Congenital malformations associated with maternal diabetes. Taiwan J Obstet Gynecol 44 (2005) 1-7
    • (2005) Taiwan J Obstet Gynecol , vol.44 , pp. 1-7
    • Chen, C.P.1
  • 7
    • 44649158271 scopus 로고    scopus 로고
    • Concomitant occurrence of holoprosencephaly and omphalocele
    • Chen C.P. Concomitant occurrence of holoprosencephaly and omphalocele. Genet Couns 19 (2008) 95-99
    • (2008) Genet Couns , vol.19 , pp. 95-99
    • Chen, C.P.1
  • 8
    • 0034107360 scopus 로고    scopus 로고
    • Genetics of ventral forebrain development and holoprosencephaly
    • Muenke M., and Beachy P.A. Genetics of ventral forebrain development and holoprosencephaly. Curr Opin Genet Dev 10 (2000) 262-269
    • (2000) Curr Opin Genet Dev , vol.10 , pp. 262-269
    • Muenke, M.1    Beachy, P.A.2
  • 9
    • 0030448727 scopus 로고    scopus 로고
    • Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly
    • Chen C.P., Liu F.F., Jan S.W., Lin C.L., and Lan C.C. Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly. Clin Genet 50 (1996) 321-326
    • (1996) Clin Genet , vol.50 , pp. 321-326
    • Chen, C.P.1    Liu, F.F.2    Jan, S.W.3    Lin, C.L.4    Lan, C.C.5
  • 10
    • 0030882884 scopus 로고    scopus 로고
    • Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly
    • Chen C.P., Lee C.C., Chen L.F., Chuang C.Y., Jan S.W., and Chen B.F. Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly. J Med Genet 34 (1997) 777-778
    • (1997) J Med Genet , vol.34 , pp. 777-778
    • Chen, C.P.1    Lee, C.C.2    Chen, L.F.3    Chuang, C.Y.4    Jan, S.W.5    Chen, B.F.6
  • 11
    • 0032831301 scopus 로고    scopus 로고
    • Prenatal diagnosis of partial trisomy 3p (3p23 pter) and monosomy 7q (7q36 qter) in a fetus with microcephaly, alobar holoprosencephaly and cyclopia
    • Chen C.P., Devriendt K., Lee C.C., Chen W.L., Wang W., and Wang T.Y. Prenatal diagnosis of partial trisomy 3p (3p23 pter) and monosomy 7q (7q36 qter) in a fetus with microcephaly, alobar holoprosencephaly and cyclopia. Prenat Diagn 19 (1999) 986-989
    • (1999) Prenat Diagn , vol.19 , pp. 986-989
    • Chen, C.P.1    Devriendt, K.2    Lee, C.C.3    Chen, W.L.4    Wang, W.5    Wang, T.Y.6
  • 12
    • 0034987246 scopus 로고    scopus 로고
    • Prenatal diagnosis of partial monosomy 18p (18p11.2 pter) and trisomy 21q (21q22.3 qter) with alobar holoprosencephaly and premaxillary agenesis
    • Chen C.P., Chern S.R., Wang W., et al. Prenatal diagnosis of partial monosomy 18p (18p11.2 pter) and trisomy 21q (21q22.3 qter) with alobar holoprosencephaly and premaxillary agenesis. Prenat Diagn 21 (2001) 346-350
    • (2001) Prenat Diagn , vol.21 , pp. 346-350
    • Chen, C.P.1    Chern, S.R.2    Wang, W.3
  • 13
    • 0036034834 scopus 로고    scopus 로고
    • Second-trimester diagnosis of digynic triploidy in a case of anhydramnios and fetal cyclopia by ultrasound-guided transabdominal chorionic villus sampling
    • Chen C.P., Hsu H.C., Chern S.R., Tzen C.Y., Wang W., and Lin C.J. Second-trimester diagnosis of digynic triploidy in a case of anhydramnios and fetal cyclopia by ultrasound-guided transabdominal chorionic villus sampling. Ultrasound Obstet Gynecol 20 (2002) 415-416
    • (2002) Ultrasound Obstet Gynecol , vol.20 , pp. 415-416
    • Chen, C.P.1    Hsu, H.C.2    Chern, S.R.3    Tzen, C.Y.4    Wang, W.5    Lin, C.J.6
  • 14
    • 16444376789 scopus 로고    scopus 로고
    • A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly
    • Chen C.P., Chern S.R., Lin C.J., Lee C.C., Wang W., and Tzen C.Y. A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly. Genet Couns 16 (2005) 49-57
    • (2005) Genet Couns , vol.16 , pp. 49-57
    • Chen, C.P.1    Chern, S.R.2    Lin, C.J.3    Lee, C.C.4    Wang, W.5    Tzen, C.Y.6
  • 15
    • 18244374414 scopus 로고    scopus 로고
    • Prenatal diagnosis of de novo partial trisomy 13q (13q22 qter) and partial monosomy 8p (8p23.3 pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart
    • Chen C.P., Chern S.R., Hsu C.Y., Lee C.C., Lee M.S., and Wang W. Prenatal diagnosis of de novo partial trisomy 13q (13q22 qter) and partial monosomy 8p (8p23.3 pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart. Prenat Diagn 25 (2005) 334-336
    • (2005) Prenat Diagn , vol.25 , pp. 334-336
    • Chen, C.P.1    Chern, S.R.2    Hsu, C.Y.3    Lee, C.C.4    Lee, M.S.5    Wang, W.6
  • 16
  • 17
    • 42949105202 scopus 로고    scopus 로고
    • Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13
    • Chen C.P., Shih J.C., Tzen C.Y., Chern S.R., Lin C.J., and Wang W. Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13. Taiwan J Obstet Gynecol 47 (2008) 95-97
    • (2008) Taiwan J Obstet Gynecol , vol.47 , pp. 95-97
    • Chen, C.P.1    Shih, J.C.2    Tzen, C.Y.3    Chern, S.R.4    Lin, C.J.5    Wang, W.6
  • 18
    • 0034526351 scopus 로고    scopus 로고
    • A digynic triploid fetus presenting with intrauterine growth restriction, severe oligohydramnios and relative macrocephaly on prenatal ultrasound
    • Chen C.P. A digynic triploid fetus presenting with intrauterine growth restriction, severe oligohydramnios and relative macrocephaly on prenatal ultrasound. Ultrasound Obstet Gynecol 16 (2000) 291-292
    • (2000) Ultrasound Obstet Gynecol , vol.16 , pp. 291-292
    • Chen, C.P.1
  • 19
    • 20444453951 scopus 로고    scopus 로고
    • Central nervous system anomalies associated with fetal trisomy 18
    • Chen C.P. Central nervous system anomalies associated with fetal trisomy 18. Prenat Diagn 25 (2005) 419-421
    • (2005) Prenat Diagn , vol.25 , pp. 419-421
    • Chen, C.P.1
  • 20
    • 34249011459 scopus 로고    scopus 로고
    • Prenatal sonographic features of trisomy 13
    • Chen C.P., and Chien S.C. Prenatal sonographic features of trisomy 13. J Med Ultrasound 15 (2007) 58-66
    • (2007) J Med Ultrasound , vol.15 , pp. 58-66
    • Chen, C.P.1    Chien, S.C.2
  • 21
    • 35348910883 scopus 로고    scopus 로고
    • Prenatal sonographic features of triploidy
    • Chen C.P., and Chien S.C. Prenatal sonographic features of triploidy. J Med Ultrasound 15 (2007) 175-182
    • (2007) J Med Ultrasound , vol.15 , pp. 175-182
    • Chen, C.P.1    Chien, S.C.2
  • 22
    • 0029838858 scopus 로고    scopus 로고
    • Holoprosencephaly: epidemiologic and clinical characteristics of a California population
    • Croen L.A., Shaw G.M., and Lammer E.J. Holoprosencephaly: epidemiologic and clinical characteristics of a California population. Am J Med Genet 64 (1996) 465-472
    • (1996) Am J Med Genet , vol.64 , pp. 465-472
    • Croen, L.A.1    Shaw, G.M.2    Lammer, E.J.3
  • 23
    • 0035339735 scopus 로고    scopus 로고
    • Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England
    • Bullen P.J., Rankin J.M., and Robson S.C. Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England. Am J Obstet Gynecol 184 (2001) 1256-1262
    • (2001) Am J Obstet Gynecol , vol.184 , pp. 1256-1262
    • Bullen, P.J.1    Rankin, J.M.2    Robson, S.C.3
  • 24
    • 0025812713 scopus 로고
    • Fetal holoprosencephaly: associated malformations and chromosomal defects
    • Berry S.M., Gosden C., Snijders R.J.M., and Nicolaides K.H. Fetal holoprosencephaly: associated malformations and chromosomal defects. Fetal Diagn Ther 5 (1990) 92-99
    • (1990) Fetal Diagn Ther , vol.5 , pp. 92-99
    • Berry, S.M.1    Gosden, C.2    Snijders, R.J.M.3    Nicolaides, K.H.4
  • 25
    • 0030035711 scopus 로고    scopus 로고
    • Holoprosencephaly in the west of Scotland 1975-1994
    • Whiteford M.L., and Tolmie J.L. Holoprosencephaly in the west of Scotland 1975-1994. J Med Genet 33 (1996) 578-584
    • (1996) J Med Genet , vol.33 , pp. 578-584
    • Whiteford, M.L.1    Tolmie, J.L.2
  • 29
    • 24644519874 scopus 로고    scopus 로고
    • The impact of gestational age on the sonographic detection of aneuploidy
    • Picklesimer A.H., Moise Jr. K.J., and Wolfe H.M. The impact of gestational age on the sonographic detection of aneuploidy. Am J Obstet Gynecol 193 (2005) 1243-1247
    • (2005) Am J Obstet Gynecol , vol.193 , pp. 1243-1247
    • Picklesimer, A.H.1    Moise Jr., K.J.2    Wolfe, H.M.3
  • 32
    • 0035659484 scopus 로고    scopus 로고
    • Contribution of ultrasono-graphic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe
    • De Vigan C., Baena N., Cariati E., Clementi M., Stoll C., and EUROSCAN Working Group. Contribution of ultrasono-graphic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Ann Genet 44 (2001) 209-217
    • (2001) Ann Genet , vol.44 , pp. 209-217
    • De Vigan, C.1    Baena, N.2    Cariati, E.3    Clementi, M.4    Stoll, C.5    EUROSCAN Working Group6
  • 33
    • 0026787127 scopus 로고
    • Ultrasonographically detectable markers of fetal chromosomal abnormalities
    • Nicolaides K.H., Snijders R.J.M., Gosden C.M., Berry C., and Campbell S. Ultrasonographically detectable markers of fetal chromosomal abnormalities. Lancet 340 (1992) 704-707
    • (1992) Lancet , vol.340 , pp. 704-707
    • Nicolaides, K.H.1    Snijders, R.J.M.2    Gosden, C.M.3    Berry, C.4    Campbell, S.5
  • 37
    • 0022346604 scopus 로고
    • Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks
    • Murray J.C., Johnson J.A., and Bird T.D. Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks. Clin Genet 28 (1985) 272-283
    • (1985) Clin Genet , vol.28 , pp. 272-283
    • Murray, J.C.1    Johnson, J.A.2    Bird, T.D.3
  • 39
    • 18744412353 scopus 로고    scopus 로고
    • Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion
    • Chen C.P., Chang T.Y., Shih J.C., et al. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Prenat Diagn 22 (2002) 1063-1066
    • (2002) Prenat Diagn , vol.22 , pp. 1063-1066
    • Chen, C.P.1    Chang, T.Y.2    Shih, J.C.3
  • 40
    • 0026518742 scopus 로고
    • The Dandy-Walker syndrome: the value of antenatal diagnosis
    • Cornford E., and Twining P. The Dandy-Walker syndrome: the value of antenatal diagnosis. Clin Radiology 45 (1992) 172-174
    • (1992) Clin Radiology , vol.45 , pp. 172-174
    • Cornford, E.1    Twining, P.2
  • 41
    • 0034085746 scopus 로고    scopus 로고
    • The sonographic diagnosis of Dandy-Walker and Dandy-Walker variant: associated findings and outcomes
    • Ecker J.L., Shipp T.D., Bromley B., and Benacerraf B. The sonographic diagnosis of Dandy-Walker and Dandy-Walker variant: associated findings and outcomes. Prenat Diagn 20 (2000) 328-332
    • (2000) Prenat Diagn , vol.20 , pp. 328-332
    • Ecker, J.L.1    Shipp, T.D.2    Bromley, B.3    Benacerraf, B.4
  • 42
    • 0025977254 scopus 로고
    • Enlarged cisterna magna and the Dandy-Walker malformation: factors associated with chromosome abnormalities
    • Nyberg D.A., Mahony B.S., Hegge F.N., Hickok D., Luthy D.A., and Kapur R. Enlarged cisterna magna and the Dandy-Walker malformation: factors associated with chromosome abnormalities. Obstet Gynecol 77 (1991) 436-442
    • (1991) Obstet Gynecol , vol.77 , pp. 436-442
    • Nyberg, D.A.1    Mahony, B.S.2    Hegge, F.N.3    Hickok, D.4    Luthy, D.A.5    Kapur, R.6
  • 43
    • 0024354018 scopus 로고
    • Dandy-Walker syndrome, a review of 15 cases evaluated by prenatal sonography
    • Russ P.D., Pretorius D.H., and Johnson M.J. Dandy-Walker syndrome, a review of 15 cases evaluated by prenatal sonography. Am J Obstet Gynecol 161 (1989) 401-406
    • (1989) Am J Obstet Gynecol , vol.161 , pp. 401-406
    • Russ, P.D.1    Pretorius, D.H.2    Johnson, M.J.3
  • 44
    • 0017727668 scopus 로고
    • Dandy-Walker syndrome: clinico-pathological features and re-evaluation of modes of treatment
    • Carmel P.W., Antunes J.L., Hilal S.K., and Gold A.P. Dandy-Walker syndrome: clinico-pathological features and re-evaluation of modes of treatment. Surg Neurol 8 (1977) 132-138
    • (1977) Surg Neurol , vol.8 , pp. 132-138
    • Carmel, P.W.1    Antunes, J.L.2    Hilal, S.K.3    Gold, A.P.4
  • 45
    • 0031919286 scopus 로고    scopus 로고
    • Enlarged cisterna magna in the third trimester as a clue to fetal trisomy 18
    • Chen C.P., Hung T.H., Jan S.W., and Jeng C.J. Enlarged cisterna magna in the third trimester as a clue to fetal trisomy 18. Fetal Diagn Ther 13 (1998) 29-34
    • (1998) Fetal Diagn Ther , vol.13 , pp. 29-34
    • Chen, C.P.1    Hung, T.H.2    Jan, S.W.3    Jeng, C.J.4
  • 46
    • 0028075474 scopus 로고
    • Sonographic detection of inferior vermian agenesis in Dandy-Walker malformations: prognostic implications
    • Chang M.C., Russell S.A., Callen P.W., Filly R.A., and Goldstein R.B. Sonographic detection of inferior vermian agenesis in Dandy-Walker malformations: prognostic implications. Radiology 193 (1994) 765-770
    • (1994) Radiology , vol.193 , pp. 765-770
    • Chang, M.C.1    Russell, S.A.2    Callen, P.W.3    Filly, R.A.4    Goldstein, R.B.5
  • 47
    • 0030835035 scopus 로고    scopus 로고
    • Dandy-Walker malformation diagnosed before 21 weeks of gestation: associated malformations and chromosomal abnormalities
    • Ulm B., Ulm M.R., Deutinger J., and Bernaschek G. Dandy-Walker malformation diagnosed before 21 weeks of gestation: associated malformations and chromosomal abnormalities. Ultrasound Obstet Gynecol 10 (1997) 167-170
    • (1997) Ultrasound Obstet Gynecol , vol.10 , pp. 167-170
    • Ulm, B.1    Ulm, M.R.2    Deutinger, J.3    Bernaschek, G.4
  • 48
    • 0022522868 scopus 로고
    • Neural tube defects in spontaneous abortions
    • Byrne J., and Warburton D. Neural tube defects in spontaneous abortions. Am J Med Genet 25 (1986) 327-333
    • (1986) Am J Med Genet , vol.25 , pp. 327-333
    • Byrne, J.1    Warburton, D.2
  • 49
    • 0036936531 scopus 로고    scopus 로고
    • Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report
    • Phadke S.R., and Thakur S. Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report. Prenat Diagn 22 (2002) 1240-1241
    • (2002) Prenat Diagn , vol.22 , pp. 1240-1241
    • Phadke, S.R.1    Thakur, S.2
  • 50
    • 27944480484 scopus 로고    scopus 로고
    • Iniencephaly and chromo-some mosaicism: a report of two cases
    • Halder A., Agarwal S., and Pandey A. Iniencephaly and chromo-some mosaicism: a report of two cases. Congenit Anom (Kyoto) 45 (2005) 102-105
    • (2005) Congenit Anom (Kyoto) , vol.45 , pp. 102-105
    • Halder, A.1    Agarwal, S.2    Pandey, A.3
  • 53
    • 0029027715 scopus 로고
    • Neural tube defects, chromosome abnormalities and multiple closure sites for the human neural tube
    • Seller M.J. Neural tube defects, chromosome abnormalities and multiple closure sites for the human neural tube. Clin Dysmorphol 4 (1995) 202-207
    • (1995) Clin Dysmorphol , vol.4 , pp. 202-207
    • Seller, M.J.1
  • 54
    • 0004715158 scopus 로고
    • Cleft lip and palate: etiology and pathogenesis
    • Kernahan D.A., Rosenstein S.W., and Dado D.V. (Eds), Williams & Wilkins, Baltimore
    • Melnick M. Cleft lip and palate: etiology and pathogenesis. In: Kernahan D.A., Rosenstein S.W., and Dado D.V. (Eds). Cleft Lip and Palate: A System of Management (1990), Williams & Wilkins, Baltimore 3-12
    • (1990) Cleft Lip and Palate: A System of Management , pp. 3-12
    • Melnick, M.1
  • 56
    • 0020630254 scopus 로고
    • What else to look for in a child born with a cleft of the lip and/or palate
    • Pashayan H.M. What else to look for in a child born with a cleft of the lip and/or palate. Cleft Palate J 20 (1983) 54-82
    • (1983) Cleft Palate J , vol.20 , pp. 54-82
    • Pashayan, H.M.1
  • 58
    • 0029062635 scopus 로고
    • Fetal cleft lip with and without cleft palate: US classification and correlation with outcome
    • Nyberg D.A., Sickler G.K., Hegge F.N., Kramer D.J., and Kropp R.J. Fetal cleft lip with and without cleft palate: US classification and correlation with outcome. Radiology 195 (1995) 677-684
    • (1995) Radiology , vol.195 , pp. 677-684
    • Nyberg, D.A.1    Sickler, G.K.2    Hegge, F.N.3    Kramer, D.J.4    Kropp, R.J.5
  • 59
    • 0033652915 scopus 로고    scopus 로고
    • Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries
    • Clementi M., Tenconi R., Bianchi F., Stoll C., and EUROSCAN study group. Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries. Prenat Diagn 20 (2000) 870-875
    • (2000) Prenat Diagn , vol.20 , pp. 870-875
    • Clementi, M.1    Tenconi, R.2    Bianchi, F.3    Stoll, C.4    EUROSCAN study group5
  • 60
    • 0035161952 scopus 로고    scopus 로고
    • Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses
    • Bergé S.J., Plath H., Van De Vondel P.T., et al. Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses. Ultrasound Obstet Gynecol 18 (2001) 422-431
    • (2001) Ultrasound Obstet Gynecol , vol.18 , pp. 422-431
    • Bergé, S.J.1    Plath, H.2    Van De Vondel, P.T.3
  • 61
    • 0034120892 scopus 로고    scopus 로고
    • Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination
    • Stoll C., Dott B., Alembik Y., and Roth M. Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination. Ann Genet 43 (2000) 11-14
    • (2000) Ann Genet , vol.43 , pp. 11-14
    • Stoll, C.1    Dott, B.2    Alembik, Y.3    Roth, M.4
  • 62
    • 0035167911 scopus 로고    scopus 로고
    • Prevalence of aneuploidy and additional anatomic abnormalities in fetuses and neonates with cleft lip with or without cleft palate: a population-based study in Utah
    • Walker S.J., Ball R.H., Babcook C.J., and Feldkamp M.M. Prevalence of aneuploidy and additional anatomic abnormalities in fetuses and neonates with cleft lip with or without cleft palate: a population-based study in Utah. J Ultrasound Med 20 (2001) 1175-1180
    • (2001) J Ultrasound Med , vol.20 , pp. 1175-1180
    • Walker, S.J.1    Ball, R.H.2    Babcook, C.J.3    Feldkamp, M.M.4
  • 63


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.