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Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population
BACKGROUND: Genetic causes of male infertility are hypothesized to involve multiple types of mutations, from single gene defects to complex chromosome rearrangements. Recently, several recurrent X-chromosome microdeletions (located in subtelomeric region of the long arm) were reported to be associat...
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| Publicat a: | PLoS One |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4892532/ https://ncbi.nlm.nih.gov/pubmed/27257673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0156102 |
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