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

Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.

Fertility and sterility - 1 Nov 2010

Havasi Viktoria, Rowe Steven M, Kolettis Peter N, Dayangac Didem, Sahin Ahmet, Grangeia Ana, Carvalho Filipa, Barros Alberto, Sousa Mario, Bassas Lluis, Casals Teresa, Sorscher Eric J

Abstract excerpt

OBJECTIVE: To investigate whether genetic modifiers of cystic fibrosis (CF) lung disease also predispose to congenital bilateral absence of the vas deferens (CBAVD) in association with cystic fibrosis transmembrane conductance regulator (CFTR) mutations. We tested the hypothesis that polymorphism...

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 Penetrance

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Receptor, Endothelin A

Share to Transforming Growth Factor beta1

Share to Turkey

Share to Urogenital Abnormalities

Share to Vas Deferens

Source

Open in PubMed Open full text

Identifiers

PMID: 20100616
DOI: 10.1016/j.fertnstert.2009.11.044
PMCID: PMC3767313

Genes

CFTR
EDNRA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20100616-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.PMID 20100616Read ↗

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

Mutations of the CFTR gene in Turkish patients 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 ↗

Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa.Semantic proximity Read ↗

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosisSemantic 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 ↗

Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants.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 ↗

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

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

Congenital Bilateral Absence of the Vas DeferensSemantic proximity Read ↗

[Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients].Semantic proximity Read ↗

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