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Volumn 30, Issue 4, 2010, Pages 329-332

Outcome of pregnancies with trisomy 2 cells in chorionic villi

Author keywords

Chorionic villous sampling; Confined placental mosaicism; Fetal growth restriction; Trisomy 2

Indexed keywords

ADULT; AMNIOCENTESIS; AORTA COARCTATION; ARTICLE; BIRTH WEIGHT; CHORION VILLUS; CHORION VILLUS SAMPLING; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GESTATIONAL AGE; HUMAN; INTRAUTERINE GROWTH RETARDATION; MEDICAL RECORD; NEWBORN; PREGNANCY OUTCOME; PRIORITY JOURNAL; TRISOMY; TRISOMY 2; ULTRASOUND;

EID: 77950634539     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2457     Document Type: Article
Times cited : (25)

References (20)
  • 3
    • 0035085635 scopus 로고    scopus 로고
    • Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)
    • Albrecht B, Mergenthaler S, Eggermann K, Zerres K, Passarge E, Eggermann T. 2001. Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q). J Med Genet 38: 214-215.
    • (2001) J Med Genet , vol.38 , pp. 214-215
    • Albrecht, B.1    Mergenthaler, S.2    Eggermann, K.3    Zerres, K.4    Passarge, E.5    Eggermann, T.6
  • 4
    • 0031044565 scopus 로고    scopus 로고
    • Trisomy 2: Confined placental mosaicism in a fetus with intrauterine growth retardation
    • Ariel I, Lerer I, Yagel S, Cohen R, Ben-Neriah Z, Abeliovich D. 1997. Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardation. Prenat Diagn 17: 180-183.
    • (1997) Prenat Diagn , vol.17 , pp. 180-183
    • Ariel, I.1    Lerer, I.2    Yagel, S.3    Cohen, R.4    Ben-Neriah, Z.5    Abeliovich, D.6
  • 5
    • 1842550512 scopus 로고    scopus 로고
    • Prenatal diagnosis of chromosomal abnormalities through amniocentesis
    • Milunsky A (ed.). The John Hopkins University Press: Baltimore
    • Benn P, Hsu L. 2004. Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In Genetic Disorders of the Fetus. Diagnosis, Prevention, and Treatment, Milunsky A (ed.). The John Hopkins University Press: Baltimore; 214-296.
    • (2004) Genetic Disorders of the Fetus. Diagnosis, Prevention, and Treatment , pp. 214-296
    • Benn, P.1    Hsu, L.2
  • 6
    • 70349261209 scopus 로고    scopus 로고
    • The replacement of cytogenetic analysis by direct chorionic villi sampling preparation with quantitative fluorescence PCR
    • Christopoulou S, Christopoulou G, Hatzaki A, et al. 2009. The replacement of cytogenetic analysis by direct chorionic villi sampling preparation with quantitative fluorescence PCR. Gynecol Obstet Invest 68: 255-261.
    • (2009) Gynecol Obstet Invest , vol.68 , pp. 255-261
    • Christopoulou, S.1    Christopoulou, G.2    Hatzaki, A.3
  • 8
    • 0030915884 scopus 로고    scopus 로고
    • Confined placental mosaicism for trisomy 2 with intrauterine growth retardation and severe oligohydramnios in the absence of uniparental disomy in the fetus
    • Gibbons B, Cheng HH, Yoong AKH, Brown S. 1997. Confined placental mosaicism for trisomy 2 with intrauterine growth retardation and severe oligohydramnios in the absence of uniparental disomy in the fetus. Prenat Diagn 17: 689-690.
    • (1997) Prenat Diagn , vol.17 , pp. 689-690
    • Gibbons, B.1    Cheng, H.H.2    Yoong, A.K.H.3    Brown, S.4
  • 9
    • 33645132708 scopus 로고    scopus 로고
    • Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi
    • Grati FR, Grimi B, Frascoli G, et al. 2006. Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi. Eur J Hum Genet 14: 282-288.
    • (2006) Eur J Hum Genet , vol.14 , pp. 282-288
    • Grati, F.R.1    Grimi, B.2    Frascoli, G.3
  • 10
    • 0030986393 scopus 로고    scopus 로고
    • Accuracy of cytogenetic findings on chorionic villus sampling (CVS) - Diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992
    • Hahnemann JM, Vejerslev LO. 1997. Accuracy of cytogenetic findings on chorionic villus sampling (CVS) - diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992. Prenat Diagn 17: 801-820.
    • (1997) Prenat Diagn , vol.17 , pp. 801-820
    • Hahnemann, J.M.1    Vejerslev, L.O.2
  • 11
    • 0030973681 scopus 로고    scopus 로고
    • Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: Karyotype/phenotype correlations
    • Hsu LY, Yu MT, Neu RL, et al. 1997. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: Karyotype/phenotype correlations. Prenat Diagn 17: 201-242.
    • (1997) Prenat Diagn , vol.17 , pp. 201-242
    • Hsu, L.Y.1    Yu, M.T.2    Neu, R.L.3
  • 12
    • 51949118174 scopus 로고    scopus 로고
    • First-trimester screening for trisomy 21 by free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A: Impact of maternal and pregnancy characteristics
    • Kagan KO, Wright D, Spencer K, Molina FS, Nicolaides KH. 2008. First-trimester screening for trisomy 21 by free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A: impact of maternal and pregnancy characteristics. Ultrasound Obstet Gynecol 31: 493-502.
    • (2008) Ultrasound Obstet Gynecol , vol.31 , pp. 493-502
    • Kagan, K.O.1    Wright, D.2    Spencer, K.3    Molina, F.S.4    Nicolaides, K.H.5
  • 13
    • 16944367292 scopus 로고    scopus 로고
    • Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
    • Robinson WP, Barrett IJ, Bernard L, et al. 1997. Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. Am J Hum Genet 60: 917-927.
    • (1997) Am J Hum Genet , vol.60 , pp. 917-927
    • Robinson, W.P.1    Barrett, I.J.2    Bernard, L.3
  • 14
    • 0030865836 scopus 로고    scopus 로고
    • True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities
    • Sago H, Chen E, Conte WJ, et al. 1997. True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities. Am J Med Genet 72: 343-346.
    • (1997) Am J Med Genet , vol.72 , pp. 343-346
    • Sago, H.1    Chen, E.2    Conte, W.J.3
  • 15
    • 0029848905 scopus 로고    scopus 로고
    • Analysis of nine pregnancies with confined placental mosaicism for trisomy 2
    • Shaffer LG, Langlois S, McCaskill C, et al. 1996. Analysis of nine pregnancies with confined placental mosaicism for trisomy 2. Prenat Diagn 16: 899-905.
    • (1996) Prenat Diagn , vol.16 , pp. 899-905
    • Shaffer, L.G.1    Langlois, S.2    McCaskill, C.3
  • 17
    • 8344259646 scopus 로고    scopus 로고
    • Autosomal aneuploidy
    • Gersen S, Keagle M (eds). Humana Press: Totowa
    • Wang JC. 2000. Autosomal aneuploidy. In The Principles of Clinical Cytogenetics, Gersen S, Keagle M (eds). Humana Press: Totowa; 157-190.
    • (2000) The Principles of Clinical Cytogenetics , pp. 157-190
    • Wang, J.C.1
  • 18
    • 0029797559 scopus 로고    scopus 로고
    • Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation
    • Webb AL, Sturgiss S, Warwicker P, Robson SC, Goodship JA, Wolstenholme J. 1996. Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. Prenat Diagn 16: 958-962.
    • (1996) Prenat Diagn , vol.16 , pp. 958-962
    • Webb, A.L.1    Sturgiss, S.2    Warwicker, P.3    Robson, S.C.4    Goodship, J.A.5    Wolstenholme, J.6
  • 19
    • 0035174716 scopus 로고    scopus 로고
    • Maternal uniparental heterodisomy for chromosome 2: Detection through "atypical" maternal AFP/hCG levels, with an update on a previous case
    • Wolstenholme J, White I, Sturgiss S, Carter J, Plant N, Goodship JA. 2001. Maternal uniparental heterodisomy for chromosome 2: detection through "atypical" maternal AFP/hCG levels, with an update on a previous case. Prenat Diagn 21: 813-817.
    • (2001) Prenat Diagn , vol.21 , pp. 813-817
    • Wolstenholme, J.1    White, I.2    Sturgiss, S.3    Carter, J.4    Plant, N.5    Goodship, J.A.6
  • 20
    • 0029950129 scopus 로고    scopus 로고
    • Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
    • Wolstenholme J. 1996. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization. Prenat Diagn 16: 511-524.
    • (1996) Prenat Diagn , vol.16 , pp. 511-524
    • Wolstenholme, J.1


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