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Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population
BACKGROUND: The Hereditary Breast and Ovarian Cancer Syndrome (HBOC) occurs in families with a history of breast/ovarian cancer, presenting an autosomal dominant inheritance pattern. BRCA1 and BRCA2 are high penetrance genes associated with an increased risk of up to 20-fold for breast and ovarian c...
Tallennettuna:
Julkaisussa: | BMC Med Genomics |
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Päätekijät: | , , , , , , , , , , , , , , , , |
Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
BioMed Central
2020
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7011249/ https://ncbi.nlm.nih.gov/pubmed/32039725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0652-y |
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