The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data

By Dohle GR  

Human Reproduction, Vol. 14, Iss. 2, 1999-02 ,pp. : 371-374

Oxford University Press

Access to resources Recommend Favorite

Genetics and genetic diagnosis. Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection

By Phillipson G.T.M.  

Human Reproduction, Vol. 15, Iss. 2, 2000-02 ,pp. : 431-435

Oxford University Press

Access to resources Recommend Favorite

Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling

By Ratbi Ilham   Legendre Marie   Niel Florence   Martin Josiane   Soufir Jean-Claude   Izard Vincent   Costes Bruno   Costa Catherine   Goossens Michel   Girodon Emmanuelle  

Human Reproduction, Vol. 22, Iss. 5, 2007-05 ,pp. : 1285-1291

Oxford University Press

Access to resources Recommend Favorite

Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens

By Lee Chia-Huei   Wu Chien-Chih   Wu Yi-No   Chiang Han-Sun  

Human Reproduction, Vol. 24, Iss. 3, 2009-03 ,pp. : 748-755

Oxford University Press

Access to resources Recommend Favorite

Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens

By Wu Chien-Chih  

Human Reproduction, Vol. 20, Iss. 9, 2005-09 ,pp. : 2470-2475

Oxford University Press

Access to resources Recommend Favorite