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

EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.

Andrology - 1 Jan 2014

Krausz C, Hoefsloot L, Simoni M, Tüttelmann F

Abstract excerpt

The molecular diagnosis of Y-chromosomal microdeletions is a common routine genetic test which is part of the diagnostic workup of azoospermic and severe oligozoospermic men. Since 1999, the European Academy of Andrology (EAA) and the European Molecular Genetics Quality Network (EMQN) have been a...

Read the complete abstract on PubMed

Topics

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

Share to Azoospermia
Share to Chromosomes, Human, Y
Share to Genetic Counseling

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotyping Techniques

Share to Infertility, Male

Share to Molecular Diagnostic Techniques

Share to Oligospermia

Share to Sex Chromosome Aberrations

Source

Open in PubMed Open full text

Identifiers

PMID: 24357628
DOI: 10.1111/j.2047-2927.2013.00173.x
PMCID: PMC4065365

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24357628-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.PMID 24357628Read ↗

EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004.Semantic proximity Read ↗

EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: State of the art 2023Semantic proximity Read ↗

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

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

Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory.Semantic proximity Read ↗

Y chromosome microdeletion screening in infertile men.Semantic proximity Read ↗

Y-microdeletions: a review of the genetic basis for this common cause of male infertilitySemantic proximity Read ↗

Molecular genetic analysis of 1,980 cases of male infertilitySemantic proximity Read ↗

INCIDENCE OF MICRODELETIONS IN THE AZF REGION OF THE Y CHROMOSOME IN SLOVAK PATIENTS WITH AZOOSPERMIASemantic proximity Read ↗

Clinical Review#: State of the art for genetic testing of infertile men.Semantic proximity Read ↗

Prognostic value of Y deletion analysis. The role of current methods.Semantic proximity Read ↗

Cellular and Molecular Genetic Analysis of 1980 Male Infertility PatientsSemantic proximity Read ↗

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