Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

By Grangeia Ana  

Human Reproduction, Vol. 19, Iss. 11, 2004-11 ,pp. : 2502-2508

Oxford University Press

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Cystic fibrosis transmembrane conductance regulator gene screening and clinical correlation in Taiwanese males with congenital bilateral absence of the vas deferens

By Wu C.C.  

Human Reproduction, Vol. 19, Iss. 2, 2004-02 ,pp. : 250-253

Oxford University Press

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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

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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

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

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

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