Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Congenital bilateral absence of vas deferens in the absence of cystic fibrosis.

Lancet (London, England) - 26 Nov 1994

Augarten A, Yahav Y, Kerem B S, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E, Madgar I

Abstract excerpt

The high frequency of mutations in the cystic fibrosis gene in patients with congenital bilateral absence of vas deferens (CBAVD) has raised the question whether all of them have a genital form of cystic fibrosis. We investigated 47 CBAVD patients by ultrasonography, 10 (21%) had renal malformations and 37 (79%) did not. In the former group, no cystic fibrosis mutations were found and sweat chloride...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cystic Fibrosis
Share to Infertility, Male
Share to Kidney

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Ultrasonography

Share to Vas Deferens

Source

Identifiers

PMID: 7968122
DOI: 10.1016/s0140-6736(94)90292-5

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital bilateral absence of vas deferens in the absence of cystic fibrosis.PMID 7968122Read ↗

Correlation between genito-urinary anomalies, semen analysis and CFTR genotype in patients with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling.Semantic proximity Read ↗

Congenital absence of vas deferens and cystic fibrosis.Semantic proximity Read ↗

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

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferensSemantic proximity Read ↗

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens.Semantic proximity Read ↗

Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).Semantic proximity Read ↗

Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counselingSemantic proximity Read ↗

Congenital Bilateral Absence of the Vas DeferensSemantic proximity Read ↗

Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.Semantic proximity Read ↗

Congenital absence of the vas deferens: incomplete penetrance of cystic fibrosis gene mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.