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

Oxford University Press

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Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

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Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens

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

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