메뉴 건너뛰기




Volumn , Issue 23, 1998, Pages 2686-2693

Klinfelter's syndrome; a common but poorly known sex chromosome anomaly;Klinefelters syndrom drabbar pojkar: Underdiagnostiserad kromosomrubbning

Author keywords

[No Author keywords available]

Indexed keywords

TESTOSTERONE;

EID: 0032478889     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (14)
  • 3
    • 0025561058 scopus 로고
    • Androgen therapy in Klinefelter syndrome during adolescence
    • Winter JSD. Androgen therapy in Klinefelter syndrome during adolescence. Birth Defects: Original Article Series 1991; 26: 235-45.
    • (1991) Birth Defects: Original Article Series , vol.26 , pp. 235-245
    • Winter, J.S.D.1
  • 5
    • 0026065297 scopus 로고
    • Screening for fra(x) mutation and Klinefelter syndrome in mental institutions
    • Pecile V, Filippi G. Screening for fra(x) mutation and Klinefelter syndrome in mental institutions. Clin Genet 1991; 39: 189-93.
    • (1991) Clin Genet , vol.39 , pp. 189-193
    • Pecile, V.1    Filippi, G.2
  • 6
    • 0025551161 scopus 로고
    • Edinburgh study of growth and development of children with sex chromosome abnormalities IV
    • Ratcliffe SG, Butler GE, Jones M. Edinburgh study of growth and development of children with sex chromosome abnormalities IV. Birth Defects: Original Article Series 1991; 26: 1-44.
    • (1991) Birth Defects: Original Article Series , vol.26 , pp. 1-44
    • Ratcliffe, S.G.1    Butler, G.E.2    Jones, M.3
  • 7
    • 0022002973 scopus 로고
    • Pituitarygonadal function in Klinefelter syndrome before and during puberty
    • Salbenblatt JA, Bender BG, Puck MH, Robinson A, Faiman C, Winter JSD. Pituitarygonadal function in Klinefelter syndrome before and during puberty. Pediatr Res 1985; 19: 82-6.
    • (1985) Pediatr Res , vol.19 , pp. 82-86
    • Winter, J.S.D.1
  • 8
    • 0028107779 scopus 로고
    • Mental retardation and Ulrich-Turners syndrome in cases with 45,X/46,X,+mar: Additional support for the loss of the inactivation center hypothesis
    • Cole H, Huang B, Salbert BA, Brown J, Howard-Peebles PN, Black SH et al. Mental retardation and Ulrich-Turners syndrome in cases with 45,X/46,X,+mar: Additional support for the loss of the inactivation center hypothesis. Am J Med Genet 1994; 52: 136-45.
    • (1994) Am J Med Genet , vol.52 , pp. 136-145
    • Cole, H.1    Huang, B.2    Salbert, B.A.3    Brown, J.4    Howard-Peebles, P.N.5    Black, S.H.6
  • 9
    • 0028091740 scopus 로고
    • Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq-karyotype
    • Lahn BT, Ma N, Breg WR, Stratton R, Surti U, Page D. Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq-karyotype. Nat Genet 1994; 8: 243-50.
    • (1994) Nat Genet , vol.8 , pp. 243-250
    • Lahn, B.T.1    Ma, N.2    Breg, W.R.3    Stratton, R.4    Surti, U.5    Page, D.6
  • 10
    • 0016426218 scopus 로고
    • Plasma testosterone in Klinefelter's syndrome: Diurnal variation and response to ACTH and dexamethasone
    • Smals AGH, Kloppenborg PWC, Benraad TJ. Plasma testosterone in Klinefelter's syndrome: Diurnal variation and response to ACTH and dexamethasone. Acta Endocrinol 1975; 78: 604-12.
    • (1975) Acta Endocrinol , vol.78 , pp. 604-612
    • Smals, A.G.H.1    Kloppenborg, P.W.C.2    Benraad, T.J.3
  • 11
    • 0030579607 scopus 로고    scopus 로고
    • Pinpointing the centre
    • Lyon MF. Pinpointing the centre. Nature 1996; 379: 116-7.
    • (1996) Nature , vol.379 , pp. 116-117
    • Lyon, M.F.1
  • 13
    • 16944366964 scopus 로고    scopus 로고
    • Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
    • Skuse DH, James RS, Bishop DVM, Coppin B, Dalton P, Aamodt-Leeper G et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997; 387: 705-8.
    • (1997) Nature , vol.387 , pp. 705-708
    • Skuse, D.H.1    James, R.S.2    Bishop, D.V.M.3    Coppin, B.4    Dalton, P.5    Aamodt-Leeper, G.6
  • 14
    • 0030940217 scopus 로고    scopus 로고
    • Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
    • Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A et al. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat Genet 1997; 16: 54-63.
    • (1997) Nat Genet , vol.16 , pp. 54-63
    • Rao, E.1    Weiss, B.2    Fukami, M.3    Rump, A.4    Niesler, B.5    Mertz, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.