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Volumn 19, Issue 6, 2004, Pages 488-490

Prenatal diagnosis of trisomy 2 mosaicism: A case report

Author keywords

Genetic counseling; Prenatal diagnosis; Trisomy 2 mosaicism

Indexed keywords

AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME MOSAICISM; ECHOGRAPHY; FEMALE; FETUS; GESTATIONAL AGE; HUMAN; KARYOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; STANDARDIZATION; TRISOMY; TRISOMY 2 MOSAICISM;

EID: 8344263987     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000080160     Document Type: Article
Times cited : (8)

References (10)
  • 1
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    • 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, Van Dyke DL, Benn PA, Bradshaw CL, et al: Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: Karyotype/phenotype correlations. Prenat Diagn 1997;17:201-242.
    • (1997) Prenat Diagn , vol.17 , pp. 201-242
    • Hsu, L.Y.1    Yu, M.T.2    Neu, R.L.3    Van Dyke, D.L.4    Benn, P.A.5    Bradshaw, C.L.6
  • 2
    • 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, Cox VA, Goldberg JD, Lebo RV, et al: True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities. Am J Med Genet 1997;72:343-346
    • (1997) Am J Med Genet , vol.72 , pp. 343-346
    • Sago, H.1    Chen, E.2    Conte, W.J.3    Cox, V.A.4    Goldberg, J.D.5    Lebo, R.V.6
  • 3
    • 1842415436 scopus 로고
    • Tissue specific trisomy 2 mosaicism in an infant with Pfeiffer syndrome-like features
    • abstr 538
    • Cramer AE, Richkind K, Schlam M, Muenke M, Amirkhan N: Tissue specific trisomy 2 mosaicism in an infant with Pfeiffer syndrome-like features. Am J Hum Genet 1993;53(suppl 3):abstr 538.
    • (1993) Am J Hum Genet , vol.53 , Issue.3 SUPPL.
    • Cramer, A.E.1    Richkind, K.2    Schlam, M.3    Muenke, M.4    Amirkhan, N.5
  • 4
    • 0002232454 scopus 로고
    • Prenatal diagnosis of chromosomal abnormalities through amniocentesis
    • Milunsky A (ed): Baltimore, Johns Hopkins University Press
    • Hsu LYF: Prenatal diagnosis of chromosomal abnormalities through amniocentesis; in Milunsky A (ed): Genetic Disorders and the Fetus. Baltimore, Johns Hopkins University Press, 1992, pp 155-210.
    • (1992) Genetic Disorders and the Fetus , pp. 155-210
    • Hsu, L.Y.F.1
  • 5
    • 0029077269 scopus 로고
    • Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture
    • Harrison K, Eisenger K, Anyane-Yeboa K, Brown S: Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture. Am J Med Genet 1995;58:147-151.
    • (1995) Am J Med Genet , vol.58 , pp. 147-151
    • Harrison, K.1    Eisenger, K.2    Anyane-Yeboa, K.3    Brown, S.4
  • 6
    • 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: Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. Prenat Diagn 1996;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
  • 7
    • 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, Rao KW, Chescheir NC, Aylsworth AS, et al: 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 1997;17:443-450.
    • (1997) Prenat Diagn , vol.17 , pp. 443-450
    • Hansen, W.F.1    Bernard, L.E.2    Langlois, S.3    Rao, K.W.4    Chescheir, N.C.5    Aylsworth, A.S.6
  • 8
    • 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: Maternal uniparental heterodisomy for chromosome 2: Detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case. Prenat Diagn 2001;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
  • 9
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    • Autosomal aneuploidy
    • Gersen S, Keagle M (eds): Totowa, Humana Press
    • Wang JC: Autosomal aneuploidy; in Gersen S, Keagle M (eds): The Principles of Clinical Cytogenetics. Totowa, Humana Press, 2000, pp 157-190.
    • (2000) The Principles of Clinical Cytogenetics , pp. 157-190
    • Wang, J.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.