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pro vyhledávání: '"Samantha B. Draves"'
Autor:
Jocelyn N. Plowman, Evanjalina J. Matoy, Lavanya V. Uppala, Samantha B. Draves, Cynthia J. Watson, Bridget A. Sefranek, Mark L. Stacey, Samuel P. Anderson, Michael A. Belshan, Elizabeth E. Blue, Chad D. Huff, Yusi Fu, Holly A.F. Stessman
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100306- (2024)
Summary: Approximately 20% of breast cancer cases are attributed to increased family risk, yet variation in BRCA1/2 can only explain 20%–25% of cases. Historically, only single gene or single variant testing were common in at-risk family members, a
Externí odkaz:
https://doaj.org/article/c20ab52b19624c2ebea28cfd72751227
