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Association between family history, mutation locations, and prevalence of BRCA1 or 2 mutations in ovarian cancer patients
We investigated the prevalence of germline BRCA mutations in a population‐based cohort of Austrian women diagnosed with ovarian cancer and its association with family history of cancer. We prospectively collected family pedigrees of 443 Austrian ovarian cancer patients who had been tested for the pr...
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| Publicado en: | Cancer Med |
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| Autores principales: | , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6488144/ https://ncbi.nlm.nih.gov/pubmed/30821131 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cam4.2000 |
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