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Article

[The detection of CFTR gene mutation in patients with azoospermia].

Ginekologia polska - 1 Jun 1998

Semczuk M, Kostuch M, Krzyzanowski A, Kwaśniewska A, Wojcierowski J

Abstract excerpt

Cystic fibrosis (CF) is the most common autosomal recessive disorder in Caucasian population that involves the lungs, pancreas, sweat glands, intestine, liver and reproductive tract. The majority of men with CF are infertile due to a bilateral congenital absence of the vas deferens (CBAVD). The purpose of the research was to evaluate the occurrence frequency of alleles of CFTR gene in patients with azoospermia....

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Share to Chromosome Aberrations
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9695373

Genes

CFTR
LIPA
PRL

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

[The detection of CFTR gene mutation in patients with azoospermia].PMID 9695373Read ↗

[Identification of mutation and polymorphic changes in the CFTR gene of patients with obstructive azoospermia].Semantic proximity Read ↗

[Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].Semantic proximity Read ↗

[The analysis of CFTR mutations in men with azoospermia, oligozoospermia and asthenozoospermia].Semantic proximity Read ↗

The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.Semantic proximity Read ↗

A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian PopulationSemantic proximity Read ↗

[Genetically determined male infertility caused by the CFTR gene mutations].Semantic proximity Read ↗

Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.Semantic proximity Read ↗

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

Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.Semantic proximity Read ↗

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator gene mutations in infertile males with congenital bilateral absence of the vas deferens.Semantic proximity Read ↗

Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.Semantic proximity Read ↗

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