메뉴 건너뛰기




Volumn 77, Issue 5, 2002, Pages 889-896

Relation between the anatomical genital phenotype and cystic fibrosis transmembrane conductance regulator gene mutations in the absence of the vas deferens

Author keywords

Azoospermia; CFTR gene; Male infertility; Vas deferens

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0036252580     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0015-0282(02)02954-0     Document Type: Article
Times cited : (16)

References (30)
  • 5
    • 0028069337 scopus 로고
    • The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis
    • (1994) J Androl , vol.15 , pp. 1-8
    • Oates, R.D.1    Amos, J.A.2
  • 10
    • 0027517995 scopus 로고
    • Correlation between genotype and phenotype in patients with cystic fibrosis
    • (1993) N Engl J Med , vol.329 , pp. 1308-1313
  • 15
    • 0028033069 scopus 로고
    • Population variation of common cystic fibrosis mutations. The Cystic Fibrosis Genetic Consortium
    • (1994) Hum Mutat , vol.4 , pp. 167-177
  • 16
    • 0030754623 scopus 로고    scopus 로고
    • Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF Mutation Analysis Consortium
    • (1997) Hum Mut , vol.10 , pp. 135-154
    • Estivill, X.1    Bancells, C.2    Ramos, C.3
  • 26
    • 0028069337 scopus 로고
    • The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis
    • (1994) J Androl , vol.15 , pp. 1-8
    • Oates, R.D.1    Amos, J.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.