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This book explores the genetic factors contributing to breast cancer development, including inherited gene mutations like BRCA1 and BRCA2, and their impact on risk. It covers genetic predispositions, testing methodologies, and personalized approaches to prevention and treatment based on individual genetic profiles. The role of family history in assessing risk and ethical considerations surrounding genetic testing and counseling are also discussed. A valuable resource for understanding the complex interplay between genetics and breast cancer.
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