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CNVs, Aneuploidies and Human Disease
In the perinatal setting, chromosome imbalances cause a wide range of clinically significant disorders and increase risk for other particular phenotypes. As technologies have improved to detect increasingly smaller deletions and duplications, collectively referred to as copy number variants (CNVs),...
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| Pubblicato in: | Clin Perinatol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4459515/ https://ncbi.nlm.nih.gov/pubmed/26042902 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clp.2015.03.001 |
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