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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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| Опубликовано в: : | Clin Perinatol |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2015
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| Предметы: | |
| Online-ссылка: | 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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