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Familial CRC—Beyond the Lynch Syndrome
Although 30% of individuals diagnosed with CRC report a family history of the disease, only 5–6% carry germline mutations in genes associated with known hereditary cancer syndromes. The evaluation and management of families affected with CRC can be complicated by variability in disease phenotypes an...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3926911/ https://ncbi.nlm.nih.gov/pubmed/23962553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cgh.2013.08.015 |
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