Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference22 articles.
1. Society of Gynecologic Oncology statement on risk assessment for inherited gynecologic cancer predispositions;Lancaster;Gynecol. Oncol.,2015
2. Endometrial cancer patients and compliance with genetic counseling: room for improvement;Backes;Gynecol. Oncol.,2011
3. Lynch syndrome screening should be considered for all patients with newly diagnosed endometrial cancer;Mills;Am. J. Surg. Pathol.,2014
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1. Impact of barriers and motivators on intention and confidence to undergo hereditary cancer genetic testing;Journal of Genetic Counseling;2024-05-27
2. Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients;Cancers;2024-02-04
3. PHLPP1 inhibits the growth and aerobic glycolysis activity of human ovarian granular cells through inactivating AKT pathway;BMC Women's Health;2024-01-06
4. Germline Testing Around the Globe: Challenges in Different Practice Settings;American Society of Clinical Oncology Educational Book;2023-05
5. A practical method for integrating community priorities in planning and implementing cancer control programs;Cancer Causes & Control;2023-04-18
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