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Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
BACKGROUND: Women with breast cancer who have multiple affected relatives are more likely to have inherited genetic risk factors for the disease. All the currently known genetic risk factors for breast cancer account for less than half of the average familial risk. Furthermore, the genetic factor(s)...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Breast Cancer Res |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5356248/ https://ncbi.nlm.nih.gov/pubmed/28302160 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13058-017-0825-6 |
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