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- W2117017804 abstract "BackgroundPatients with inherited mutations in one or both of the BRCA1/ BRCA2 genes are at substantially higher risk for developing breast cancer and other malignancies. Subsequent to testing becoming publicly available in the late 1990s, organizations such as the National Comprehensive Cancer Network (NCCN) developed guidelines to aid in the identification of high-probability mutation carriers. It is unclear, however, how closely such guidelines are followed by healthcare providers, or what testing barriers may exist among patients. Furthermore, little is known about the clinical care and surveillance received by patients after testing positive for a mutation. The primary objective of this study is to assemble a cohort of BRCA-tested patients, in order to examine their demographic characteristics and clinical follow-up." @default.
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- W2117017804 date "2011-11-01" @default.
- W2117017804 modified "2023-10-11" @default.
- W2117017804 title "PS2-39: Demographic Characteristics & Follow-Up Care of Patients Tested for BRCA Mutations" @default.
- W2117017804 doi "https://doi.org/10.3121/cmr.2011.1020.ps2-39" @default.
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