X Chromosome-Linked CNVs in Male Infertility: Discovery of Overall Duplication Load and Recurrent, Patient-Specific Gains with Potential Clinical Relevance-Reference-Cited by-同舟云学术

X Chromosome-Linked CNVs in Male Infertility: Discovery of Overall Duplication Load and Recurrent, Patient-Specific Gains with Potential Clinical Relevance

Published:2014-06-10 Issue:6 Volume:9 Page:e97746
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Chianese Chiara,Gunning Adam C.,Giachini Claudia,Daguin Fabrice,Balercia Giancarlo,Ars Elisabet,Giacco Deborah Lo,Ruiz-Castañé Eduard,Forti Gianni,Krausz Csilla

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference22 articles.

1. Male infertility: pathogenesis and clinical diagnosis;C Krausz;Best Pract Res Clin Endocrinol Metab,2011

2. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013;C Krausz;Andrology,2014

3. High resolution X chromosome-specific array-CGH detects new CNVs in infertile males;C Krausz;PLoS One,2012

4. Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome;F Tüttelmann;PLoS One,2011

5. Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1;AM Lopes;PLoS Genet,2013

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