Molecular analysis of mutations and polymorphisms in the CFTR gene in male infertility

Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

Miguel Chillón, Teresa Casals, Bernard Mercier et al. · New England Journal of Medicine · 1995 · 964 citations · Full text

WHO LABORATORY MANUAL FOR THE EXAMINATION OF HUMAN SEMEN AND SPERM‐CERVICAL MUCUS INTERACTION

International Journal of Andrology · 1996 · 902 citations · Full text

Infertility, Andrology, Fertility +8

Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA

Chin-Shyan Chu, Bruce C. Trapnell, S M Curristin et al. · Nature Genetics · 1993 · 514 citations

Variable Exon 9, Molecular Physiology, Mendelian Disorder +11

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.

Harry Cuppens, Wen‐chang Lin, Martine Jaspers et al. · Journal of Clinical Investigation · 1998 · 391 citations · Full text

Engineering, Genetics, Human Polymorphism +20

Genetic risk factors in infertile men with severe oligozoospermia and azoospermia

Gert R. Dohle · Human Reproduction · 2002 · 360 citations · Full text