Breast and ovarian cancer risk evaluation in families with a disease-causing mutation in BRCA1/2
Germline mutations in BRCA1 and BRCA2 confer high risks of breast and ovarian cancer, and their identification allows genetic testing of at-risk relatives. However, estimates of these risks illustrate controversies, depending on the published series. The penetrance, the earlier onset of the disease...
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Main Authors: | , , , , , |
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Format: | Text |
Language: | English |
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Springer-Verlag
2010
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Subjects: | |
Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC3185985/ https://pubmed.ncbi.nlm.nih.gov/22460208 http://dx.doi.org/10.1007/s12687-010-0014-0 |
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