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Article

Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia

1 Mar 2003

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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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PMID: 12711808
DOI: 10.1007/bf02706215

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Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermiaPMID 12711808Read ↗

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Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast TurkeySemantic proximity Read ↗

Analysis of Y Chromosome Microdeletion and Karyotype in 516 Patients With AzoospermiaSemantic proximity Read ↗

Y-Chromosome Microdeletions: A Review of Prevalence, Screening, and Clinical ConsiderationsSemantic proximity Read ↗

A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11Semantic proximity Read ↗

Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the ClinicSemantic proximity Read ↗

An analysis of the frequency of Y‐chromosome microdeletions and the determination of a threshold sperm concentration for genetic testing in infertile menSemantic proximity Read ↗

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Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy.Semantic proximity Read ↗

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