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

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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

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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Unilateral renal agenesis associated with congenital bilateral absence of the vas deferens: phenotypic findings and genetic considerations

By McCallum T.J.  

Human Reproduction, Vol. 16, Iss. 2, 2001-02 ,pp. : 282-288

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Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens

By Sharma N.   Acharya N.   Singh S.K.   Singh M.   Sharma U.   Prasad R.  

Human Reproduction, Vol. 24, Iss. 5, 2009-05 ,pp. : 1229-1236

Oxford University Press

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