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Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population
BACKGROUND: About 5–10% of breast/ovarian cancers are hereditary. However, for a large proportion of cases (around 50%), the genetic cause remains unknown. These cases are grouped in a separated BRCAX category. The aim of this study was to identify genomic alterations in BRCA1/BRCA2 wild-type tumor...
Gorde:
| Argitaratua izan da: | Oncotarget |
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| Egile Nagusiak: | , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Impact Journals LLC
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6007956/ https://ncbi.nlm.nih.gov/pubmed/29938003 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.25537 |
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