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Volumn 23, Issue 7, 2003, Pages 564-565

A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome

Author keywords

Confined placental mosaicism; Trisomy 2

Indexed keywords

ALPHA FETOPROTEIN;

EID: 0041765642     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.644     Document Type: Article
Times cited : (15)

References (9)
  • 1
    • 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
  • 2
    • 0028244914 scopus 로고
    • Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of UK data
    • Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis. 1994. Cytogenetic analysis of chorionic villi for prenatal diagnosis: an ACC collaborative study of UK data. Prenat Diagn 14: 363-379.
    • (1994) Prenat Diagn , vol.14 , pp. 363-379
  • 3
    • 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
  • 4
    • 0028231090 scopus 로고
    • The 1993-94 Genethon human genetic linkage map
    • Gyapay G, Morissette J, Vignal A, et al. 1994. The 1993-94 Genethon human genetic linkage map. Nat Genet 7(2): 246-339.
    • (1994) Nat Genet , vol.7 , Issue.2 , pp. 246-339
    • Gyapay, G.1    Morissette, J.2    Vignal, A.3
  • 5
    • 0030950624 scopus 로고    scopus 로고
    • Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios
    • Hansen WF, Bernard LE, Langlois S, et al. 1997. Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios. Prenat Diagn 17: 443-450.
    • (1997) Prenat Diagn , vol.17 , pp. 443-450
    • Hansen, W.F.1    Bernard, L.E.2    Langlois, S.3
  • 6
    • 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
  • 7
    • 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
  • 8
    • 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
  • 9
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.