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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

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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

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

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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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