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 absence of the vas deferens: a mild form of cystic fibrosis.

Molecular medicine today - 1 Jan 1996

Patrizio P, Zielenski J

Abstract excerpt

Genetic diseases presenting with different phenotypes are generally classified as distinct disorders before their molecular defect is revealed, as exemplified by the recent advance in understanding of the molecular biology of cystic fibrosis and an obstructive form of infertility, known as congen...

Topics

Congenital Abnormalities
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Genetic Variation
Genitalia, Male
Genotype
Humans
Male
Mutation
Phenotype
Vas Deferens

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8796848
DOI: 10.1016/1357-4310(96)88755-7

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8796848-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital absence of the vas deferens: a mild form of cystic fibrosis.PMID 8796848Read ↗

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

Congenital absence of the vas deferens: Cystic fibrosis transmembrane regulatory gene mutations.Semantic proximity Read ↗

Genetics of the congenital absence of the vas deferens.Semantic proximity Read ↗

Mutations of the cystic fibrosis gene and congenital absence of the vas deferens.Semantic proximity Read ↗

Congenital absence of vas deferens and cystic fibrosis.Semantic 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 ↗

The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis.Semantic proximity Read ↗

Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.Semantic proximity Read ↗

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

Urogenital anomalies in men with congenital absence of the 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 ↗

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