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Article

A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11

29 May 1998

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9654206
DOI: 10.1007/s004390050741

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Related research

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A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11PMID 9654206Read ↗

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Cytogenetic abnormalities detected in patients with non-obstructive azoospermia and severe oligozoospermiaSemantic proximity Read ↗

Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectivesSemantic proximity Read ↗

A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.Semantic proximity Read ↗

Y-chromosome microdeletions in nonobstructive azoospermia and severe oligozoospermiaSemantic proximity Read ↗

Y chromosome microdeletions in infertile men with idiopathic oligo- or azoospermiaSemantic proximity Read ↗

Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosomeSemantic proximity Read ↗

Prevalence of Y Chromosome Microdeletions in Idiopathic Azoospermia Cases in Central Indian MenSemantic proximity Read ↗

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