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Article

The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland.

British journal of urology - 1 Jan 1997

Donat R, McNeill A S, Fitzpatrick D R, Hargreave T B

Abstract excerpt

OBJECTIVE: To examine the incidence of cystic fibrosis transmembrane-conductance regulator (CFTR) gene mutations in Scottish patients with congenital bilateral absence of the vas deferens (CBAVD). PATIENTS AND METHODS: Thirty patients with CBAVD presenting consecutively to the Edinburgh infertility clinic were examined for CFTR gene mutations. All patients were assessed clinically and tested for 15 gene mutations...

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Source

Identifiers

PMID: 9043501
DOI: 10.1046/j.1464-410x.1997.30816.x

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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