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Volumn 88, Issue 6, 1998, Pages 711-714

Prader-Willi syndrome in South African patients - Clinical and molecular diagnosis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILDHOOD DISEASE; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DNA DETERMINATION; HUMAN; LABORATORY DIAGNOSIS; PRADER WILLI SYNDROME; SCORING SYSTEM; SOUTH AFRICA;

EID: 0031830996     PISSN: 02569574     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (12)
  • 1
    • 0000927260 scopus 로고
    • Ein Syndrome von Adipositas, Kleinwuchs, Kryptochismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter
    • Prader A. Labhart A. Willi H. Ein Syndrome von Adipositas, Kleinwuchs, Kryptochismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz Med Wochenschr 1956; 86: 1260-1261.
    • (1956) Schweiz Med Wochenschr , vol.86 , pp. 1260-1261
    • Prader, A.1    Labhart, A.2    Willi, H.3
  • 2
    • 0021314588 scopus 로고
    • Prader-Willi syndrome
    • Cassidy SB. Prader-Willi syndrome. Curr Probt Pediatr 1984; 14: 1-55.
    • (1984) Curr Probt Pediatr , vol.14 , pp. 1-55
    • Cassidy, S.B.1
  • 3
    • 0025181455 scopus 로고
    • Prader-Willi syndrome: Current understanding of cause and diagnosis
    • Butler MG. Prader-Willi syndrome: Current understanding of cause and diagnosis. Am J Med Genet 1990; 35: 319-332.
    • (1990) Am J Med Genet , vol.35 , pp. 319-332
    • Butler, M.G.1
  • 4
    • 0027476242 scopus 로고
    • Prader-Willi syndrome: Consensus diagnostic criteria
    • Holm VA, Cassidy SB, Butler MG, et al. Prader-Willi syndrome: Consensus diagnostic criteria. Pediatrics 1993; 91: 398-402.
    • (1993) Pediatrics , vol.91 , pp. 398-402
    • Holm, V.A.1    Cassidy, S.B.2    Butler, M.G.3
  • 6
    • 0028917529 scopus 로고
    • A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome
    • Webb T, Clarke D, Hardy CA, Kilpatrick MW, Corbett J, Dahlitz M. A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome. J Med Genet 1995; 32: 181-185.
    • (1995) J Med Genet , vol.32 , pp. 181-185
    • Webb, T.1    Clarke, D.2    Hardy, C.A.3    Kilpatrick, M.W.4    Corbett, J.5    Dahlitz, M.6
  • 7
    • 0027930212 scopus 로고
    • A variety of genetic mechanisms are associated with Prader-Willi syndrome
    • Woodage T, Deng Z-M, Prasad M, et at. A variety of genetic mechanisms are associated with Prader-Willi syndrome. Am J Med Genet 1994; 54: 219-226.
    • (1994) Am J Med Genet , vol.54 , pp. 219-226
    • Woodage, T.1    Deng, Z.-M.2    Prasad, M.3
  • 8
    • 0029867499 scopus 로고    scopus 로고
    • Diagnostic testing for Prader-Willi and Angelman Syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee
    • B. ASHG/ASMG Report. Diagnostic testing for Prader-Willi and Angelman Syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee. Am J Hum Genet 1996; 58: 1085-1088.
    • (1996) Am J Hum Genet , vol.58 , pp. 1085-1088
  • 10
    • 0014284907 scopus 로고
    • Syndrome of hypotonia-hypomentia-hypogonadismobesity (HHHO) or Prader-Wiili syndrome
    • Zellweger H, Schneider HJ. Syndrome of hypotonia-hypomentia-hypogonadismobesity (HHHO) or Prader-Wiili syndrome. Am J Dis Child 1968; 115: 588-598.
    • (1968) Am J Dis Child , vol.115 , pp. 588-598
    • Zellweger, H.1    Schneider, H.J.2
  • 12
    • 0030021929 scopus 로고    scopus 로고
    • Down syndrome in sub-Saharan Africa
    • Christianson AL. Down syndrome in sub-Saharan Africa. J Med Genet 1996; 33: 89-92.
    • (1996) J Med Genet , vol.33 , pp. 89-92
    • Christianson, A.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.