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Volumn 22, Issue 11, 2003, Pages 1271-1275

Second-Trimester Sonographic Findings in Trisomy 22: Report of 3 Cases and Review of the Literature

Author keywords

Fetal anomalies; Prenatal diagnosis; Prenatal sonography; Trisomy 22

Indexed keywords

CHROMOSOMES; MEDICAL IMAGING; SCANNING; SKIN;

EID: 0242353967     PISSN: 02784297     EISSN: None     Source Type: Journal    
DOI: 10.7863/jum.2003.22.11.1271     Document Type: Article
Times cited : (21)

References (17)
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  • 2
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    • A cytogenetic study of 1000 spontaneous abortions
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    • (1980) Ann Hum Genet , vol.44 , pp. 151-178
    • Hassold, T.1    Chen, N.2    Funkhouser, J.3
  • 5
    • 0019522231 scopus 로고
    • Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction: Delineation of a common clinical picture and report of 9 new cases from 6 families
    • Schinzel A, Schmid W, Auf der Maur P, et al. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction: delineation of a common clinical picture and report of 9 new cases from 6 families. Hum Genet 1981; 56:249-262.
    • (1981) Hum Genet , vol.56 , pp. 249-262
    • Schinzel, A.1    Schmid, W.2    Auf der Maur, P.3
  • 6
    • 0019422087 scopus 로고
    • Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22
    • Schinzel A. Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22. Hum Genet 1981; 56:269-273.
    • (1981) Hum Genet , vol.56 , pp. 269-273
    • Schinzel, A.1
  • 7
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    • Mosaic trisomy 22: A case presentation and literature review of trisomy 22 phenotypes
    • Crowe CA, Schwartz S, Black CJ, Jaswaney V. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes. Am J Med Genet 1997; 71:406-413.
    • (1997) Am J Med Genet , vol.71 , pp. 406-413
    • Crowe, C.A.1    Schwartz, S.2    Black, C.J.3    Jaswaney, V.4
  • 12
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    • Hydrops revisited: Literature review of 1414 cases published in the 1980s
    • Machin GA. Hydrops revisited: literature review of 1414 cases published in the 1980s. Am J Med Genet 1989; 34:366-390.
    • (1989) Am J Med Genet , vol.34 , pp. 366-390
    • Machin, G.A.1
  • 13
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    • Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant
    • Kim EH, Cohen RS, Ramachandran P, Mineta AK, Babu VR. Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant. Am J Med Genet 1992; 44:437-438.
    • (1992) Am J Med Genet , vol.44 , pp. 437-438
    • Kim, E.H.1    Cohen, R.S.2    Ramachandran, P.3    Mineta, A.K.4    Babu, V.R.5
  • 16
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    • Congenital diaphragmatic hernia and hydrops: A lethal association?
    • Sydorak RM, Goldstein R, Hirose S, et al. Congenital diaphragmatic hernia and hydrops: a lethal association? J Pediatr Surg 2002; 37:1678-1680.
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    • Sydorak, R.M.1    Goldstein, R.2    Hirose, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.