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Article

Evidence for a partial deletion in the androgen receptor gene in a phenotypic male with azoospermia.

American journal of obstetrics and gynecology - 1 Dec 1991

Akin J W, Behzadian A, Tho S P, McDonough P G

Abstract excerpt

Androgen resistance is thought to vary phenotypically from a normal female to an infertile male. Previous evaluation of infertile males has been limited to androgen receptor-binding affinity. The androgen receptor gene has been isolated, cloned, and studied extensively in patients with complete androgen insensitivity syndrome, but no comparative data are available on infertile males. To address this matter, the...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1750490
DOI: 10.1016/0002-9378(91)90052-s

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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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evidence for a partial deletion in the androgen receptor gene in a phenotypic male with azoospermia.PMID 1750490Read ↗

A new point mutation of the androgen receptor gene in a patient with partial androgen resistance and severe oligozoospermia.Semantic proximity Read ↗

Molecular characterization of the androgen receptor gene in boys with hypospadias.Semantic proximity Read ↗

Molecular defects of the androgen receptor.Semantic proximity Read ↗

Genetic basis of endocrine disease. 4. The spectrum of mutations in the androgen receptor gene that causes androgen resistance.Semantic proximity Read ↗

Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review.Semantic proximity Read ↗

Mutations of androgen receptor gene in androgen insensitivity syndromes.Semantic proximity Read ↗

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status.Semantic proximity Read ↗

Mutations of the androgen receptor coding sequence are infrequent in patients with isolated hypospadias.Semantic proximity Read ↗

The first detection of complete androgen insensitivity with no mutation in the coding sequence of the androgen receptor gene.Semantic proximity Read ↗

The first analysis of exon 1 (the transactivation domain) of the androgen receptor gene in infertile men with oligospermia or azoospermia.Semantic proximity Read ↗

Azoospermia associated with a mutation in the ligand-binding domain of an androgen receptor displaying normal ligand binding, but defective trans-activation.Semantic proximity Read ↗

CAG repeat length in the androgen receptor gene is enhanced in patients with idiopathic azoospermiaSemantic proximity Read ↗

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