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Volumn 92, Issue 9, 1999, Pages 921-923

Short stature in a 46,XX male adolescent

Author keywords

[No Author keywords available]

Indexed keywords

FOLLITROPIN; GONADORELIN; GONADOTROPIN; INSULIN; LUTEINIZING HORMONE;

EID: 0032856330     PISSN: 00384348     EISSN: None     Source Type: Journal    
DOI: 10.1097/00007611-199909000-00016     Document Type: Article
Times cited : (7)

References (8)
  • 1
    • 0028876671 scopus 로고
    • SRY alone can induce normal male sexual differentiation
    • Lopez M, Torres L, Mendez JP, et al: SRY alone can induce normal male sexual differentiation. Am J Med Genet 1995; 55:356-358
    • (1995) Am J Med Genet , vol.55 , pp. 356-358
    • Lopez, M.1    Torres, L.2    Mendez, J.P.3
  • 2
    • 0019194792 scopus 로고
    • Variation in pituitary-gonadal function in two adolescent boys with 46,XX male syndrome
    • LaFranchi S, Magenis ER, Prescott GH: Variation in pituitary-gonadal function in two adolescent boys with 46,XX male syndrome. J Pediatr 1980; 97:960-962
    • (1980) J Pediatr , vol.97 , pp. 960-962
    • LaFranchi, S.1    Magenis, E.R.2    Prescott, G.H.3
  • 3
    • 0023284777 scopus 로고
    • Male infertility with chromosomal abnormalities. II. XX-male syndrome
    • Hazama M, Kondo K, Fujisawa M, et al: Male infertility with chromosomal abnormalities. II. XX-male syndrome. Hinyokika Kiyo 1987; 33:193-203
    • (1987) Hinyokika Kiyo , vol.33 , pp. 193-203
    • Hazama, M.1    Kondo, K.2    Fujisawa, M.3
  • 4
    • 0030788199 scopus 로고    scopus 로고
    • FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes
    • Rao E, Weiss B, Fukami M, et al: FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes. Hum Genet 1997; 100:236-239
    • (1997) Hum Genet , vol.100 , pp. 236-239
    • Rao, E.1    Weiss, B.2    Fukami, M.3
  • 5
    • 0030877094 scopus 로고    scopus 로고
    • PHOG, a candidate gene for development in the short stature of Turner's syndrome
    • Ellison JW, Wardak Z, Young MF, et al: PHOG, a candidate gene for development in the short stature of Turner's syndrome. Hum Mol Genet 1997; 6:1341-1347
    • (1997) Hum Mol Genet , vol.6 , pp. 1341-1347
    • Ellison, J.W.1    Wardak, Z.2    Young, M.F.3
  • 6
    • 0030940217 scopus 로고    scopus 로고
    • Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner's syndrome
    • Rao E, Weiss B, Fuami M, et al: Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner's syndrome. Nat Genet 1997; 16:54-63
    • (1997) Nat Genet , vol.16 , pp. 54-63
    • Rao, E.1    Weiss, B.2    Fuami, M.3
  • 7
    • 0032546246 scopus 로고    scopus 로고
    • X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family
    • Raynaud M, Ronce N, Ayrault AD, et al: X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family. Am J Med Genet 1998; 76:255-261
    • (1998) Am J Med Genet , vol.76 , pp. 255-261
    • Raynaud, M.1    Ronce, N.2    Ayrault, A.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.