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Article

[Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].

Srpski arhiv za celokupno lekarstvo - 1 Jan 2000

Kusić Jelena, Radojković Dragica, Maletić Vinka, Branković Snezana, Savić Ana

Abstract excerpt

INTRODUCTION: Impaired infertility of the male partner is causative or contributOry to in up to one half of all couples unable to conceive spontaneously. A considerable number of genes are now known that have an essential function in human reproduction and which, when deleted or mutated, can cause pathologic changes in the male reproductive system. Congenital bilateral absence of the vas deferens (CBAVD) is an...

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Source

Identifiers

PMID: 12073281
DOI: 10.2298/sarh0202001k

Genes

CFTR

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

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[Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].PMID 12073281Read ↗

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

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

[The detection of CFTR gene mutation in patients with azoospermia].Semantic proximity Read ↗

Involvement of CFTR gene alterations in obstructive and nonobstructive infertility in men.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 ↗

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

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator mutations in azoospermic and oligospermic men and their partners.Semantic proximity Read ↗

Molecular evaluation of CFTR sequence variants in male infertility of testicular origin.Semantic proximity Read ↗

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

Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment.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 ↗

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