Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia

1 Mar 1997

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Reproductive biology and impacts on aquatic species
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9091344
DOI: 10.1016/s0015-0282(97)80083-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermiaPMID 9091344Read ↗

Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletionsSemantic proximity Read ↗

Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermiaSemantic proximity Read ↗

High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermiaSemantic proximity Read ↗

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

Genetic defects in human azoospermiaSemantic proximity Read ↗

Absence of DAZ gene mutations in cases of non-obstructed azoospermia.Semantic proximity Read ↗

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

A decade of experience emphasizes that testing for Y microdeletions is essential in American men with azoospermia and severe oligozoospermiaSemantic proximity Read ↗

Spontaneous transmission from a father to his son of a Y chromosome microdeletion involving the deleted in azoospermia (DAZ) geneSemantic proximity Read ↗

Chromosomal abnormalities in patients with oligozoospermia and non-obstructive azoospermiaSemantic proximity Read ↗

Novel missense mutations of the Deleted-in-AZoospermia-Like (DAZL) gene in infertile women and menSemantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.