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A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype
This report highlights the necessity of genetic testing, at least for BRCA1 mutations, of young females diagnosed with triple negative breast cancer, even in the absence of or limited family history. A 34-year-old female with a locally advanced, triple negative tumour, which perforated the skin, is...
Tallennettuna:
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Hindawi Publishing Corporation
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3934306/ https://ncbi.nlm.nih.gov/pubmed/24660075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/875029 |
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