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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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

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

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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

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

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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

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Reproductive pathology. Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens

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Human Reproduction, Vol. 15, Iss. 7, 2000-07 ,pp. : 1476-1483

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