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Prospective comparison of family medical history with personal genome screening for risk assessment of common cancers
Family history-based risk assessment (FHRA) is a genetic tool for identifying those at risk of disease. Genome-wide association studies have shown that single nucleotide polymorphisms (SNP) are statistically associated with low- to moderate-level risks of diseases. There has been limited study of co...
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| Main Authors: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group
2012
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3330209/ https://ncbi.nlm.nih.gov/pubmed/22215421 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.224 |
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