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

INTRODUCTION: Spermatogenesis is a highly complex process involving several thousand genes, only a minority of which have been studied in infertile men. In a previous study, we identified a number of Copy Number Variants (CNVs) by high-resolution array-Comparative Genomic Hybridization (a-CGH) analy...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Chianese, Chiara, Gunning, Adam C., Giachini, Claudia, Daguin, Fabrice, Balercia, Giancarlo, Ars, Elisabet, Giacco, Deborah Lo, Ruiz-Castañé, Eduard, Forti, Gianni, Krausz, Csilla
التنسيق: Artigo
اللغة:Inglês
منشور في: Public Library of Science 2014
الموضوعات:
Research Article
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC4051606/
https://ncbi.nlm.nih.gov/pubmed/24914684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0097746
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