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Integrating common and rare genetic variation in diverse human populations
Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide studies that fully examine less common alleles in populations with a wide range of ancestry. To inform the design and inter...
Uloženo v:
| Médium: | Artigo |
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| Jazyk: | Inglês |
| Vydáno: |
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3173859/ https://ncbi.nlm.nih.gov/pubmed/20811451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature09298 |
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