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Volumn 347, Issue 9002, 1996, Pages 699-

Consanguinity in two seemingly unrelated patients with congenital adrenal hyperplasia [23]

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CASE REPORT; CONGENITAL ADRENAL HYPERPLASIA; CONSANGUINITY; FEMALE; HUMAN; LETTER; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0029865350     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(96)91257-X     Document Type: Letter
Times cited : (6)

References (2)
  • 1
    • 0021957268 scopus 로고
    • Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia
    • H. Vierhapper P. Nowotny W. Waldhäusl H. Frisch Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia J Steroid Biochem 3 1985 363 369
    • (1985) J Steroid Biochem , vol.3 , pp. 363-369
    • Vierhapper, H.1    Nowotny, P.2    Waldhäusl, W.3    Frisch, H.4
  • 2
    • 0026712412 scopus 로고
    • Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes
    • A. Helmberg M. Tabarelli Ma Fuchs Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes DNA Cell Biol 11 1992 359 368
    • (1992) DNA Cell Biol , vol.11 , pp. 359-368
    • Helmberg, A.1    Tabarelli, M.2    Fuchs, Ma3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.