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Human Reproduction, Vol. 19, Iss. 2, 2004-02 ,pp. : 250-253

Oxford University Press

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Genetics and genetic diagnosis. Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection

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Human Reproduction, Vol. 15, Iss. 2, 2000-02 ,pp. : 431-435

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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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The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data

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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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