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Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome
A genetic origin is estimated in 30% of infertile men with the common phenotypes of oligo- or azoospermia, but the pathogenesis of spermatogenic failure remains frequently obscure. To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Public Library of Science
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3084853/ https://ncbi.nlm.nih.gov/pubmed/21559371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0019426 |
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