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Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes
The rapid clinical embrace of next generation multigene cancer predisposition panels has resulted in discovery of DNA variants in genes for which very limited data on penetrance has been published. Evidence for increased risks associated with these genes is often expressed in odds ratios and studies...
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| Опубликовано в: : | Fam Cancer |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Springer Netherlands
2016
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4901094/ https://ncbi.nlm.nih.gov/pubmed/26960971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-016-9896-2 |
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