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The prevalence of BRCA1 mutations among young women with triple-negative breast cancer
BACKGROUND: Molecular screening for BRCA1 and BRCA2 mutations is now an established component of risk evaluation and management of familial breast cancer. Features of hereditary breast cancer include an early age-of-onset and over-representation of the 'triple-negative' phenotype (negative...
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| Main Authors: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2009
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2666759/ https://ncbi.nlm.nih.gov/pubmed/19298662 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2407-9-86 |
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