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 the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype.

Human genetics - 1 Jan 1996

Dumur V, Gervais R, Rigot J M, Delomel-Vinner E, Decaestecker B, Lafitte J J, Roussel P

Abstract excerpt

To assess better the link between congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis (CF), we compared sweat chloride values, analysis of the CFTR intron 8 poly(T) tract length and analysis of 10 exons in a population of 38 patients with CBAVD. The data indicate that thi...

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Exons
Share to CFTR gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genotype

Share to Introns

Share to Mutation

Share to Phenotype

Source

Identifiers

PMID: 8557264
DOI: 10.1007/BF00218824

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-8557264-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype.PMID 8557264Read ↗

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

Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.Semantic proximity Read ↗

Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

[Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens].Semantic proximity Read ↗

[Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].Semantic proximity Read ↗

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.Semantic proximity Read ↗

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

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

Cystic fibrosis transmembrane conductance regulator gene screening and clinical correlation in Taiwanese males with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.Semantic proximity Read ↗

Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

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