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High Resolution X Chromosome-Specific Array-CGH Detects New CNVs in Infertile Males
CONTEXT: The role of CNVs in male infertility is poorly defined, and only those linked to the Y chromosome have been the object of extensive research. Although it has been predicted that the X chromosome is also enriched in spermatogenesis genes, no clinically relevant gene mutations have been ident...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3467283/ https://ncbi.nlm.nih.gov/pubmed/23056185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0044887 |
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