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

Oxford University Press

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

By Casals Teresa  

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

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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

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