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The pathology of familial breast cancer: Clinical and genetic counselling implications of breast cancer pathology
Approximately 5% of all breast cancers are due to one of the high-risk breast cancer genes BRCA1 and BRCA2, or possibly to a third or fourth moderate- to high-risk gene(s). A further proportion of cases arise in the presence of a less striking family history, with later average age at onset and lowe...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
1999
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3386651/ https://ncbi.nlm.nih.gov/pubmed/11250683 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/bcr13 |
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