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

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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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Reproductive genetics. Cystic fibrosis phenotype evaluation and paternity outcome in 50 males with congenital bilateral absence of vas deferens

By Josserand Raphaële Nove  

Human Reproduction, Vol. 16, Iss. 10, 2001-10 ,pp. : 2093-2097

Oxford University Press

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Analysis by mass spectrometry of 100 cystic fibrosis gene mutations in 92 patients with congenital bilateral absence of the vas deferens

By Wang Zhenyuan  

Human Reproduction, Vol. 17, Iss. 8, 2002-08 ,pp. : 2066-2072

Oxford University Press

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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

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