Congenital bilateral absence of the vas
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R. D. Oates; J. A. Amos
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Article
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1993
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Springer-Verlag
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English
β 798 KB
CF and CBAVD are really just ends of a clinical spectrum. The type and nature of the mutations in the CF gene probably determine the phenotypic expression of the patient. Perhaps all patients homozygous for AF508, for example, will have severe pulmonary and pancreatic disease as well as absent vasa,