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SEOM clinical guidelines in Hereditary Breast and ovarian cancer
Approximately, 7 % of all breast cancers (BC) and 11–15 % of ovarian cancers (OC) are associated with inherited predisposition, mainly related to germline mutations in high penetrance BRCA1/2 genes. Clinical criteria for genetic testing are based on personal and family history to estimate a minimum...
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| Publicat a: | Clin Transl Oncol |
|---|---|
| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Milan
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4689749/ https://ncbi.nlm.nih.gov/pubmed/26669313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12094-015-1435-3 |
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