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BRCA1/2 MUTATIONS AND TRIPLE NEGATIVE BREAST CANCERS
Identifying breast cancer patients at increased risk for carrying a mutation in the BRCA1 and BRCA2 genes is an important objective in clinical practice. Although age at diagnosis, family history of breast and/or ovarian cancer, and ethnicity are all essential parameters to consider when assessing r...
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3870050/ https://ncbi.nlm.nih.gov/pubmed/21778580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/BD-2010-0306 |
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