Hereditary Syndromes Manifesting as Endometrial Carcinoma: How Can Pathological Features Aid Risk Assessment?

• المؤلفون الرئيسيون: Wong, A, Ngeow, J
• مؤلفون آخرون: DUKE-NUS MEDICAL SCHOOL
• التنسيق: Review
• منشور في: 2020
• الموضوعات: BRCA1 protein; BRCA2 protein; cancer epidemiology; cancer patient; cancer risk; Cowden syndrome; endometrium carcinoma; female; gene; gene mutation; hereditary nonpolyposis colorectal cancer; human; immunohistochemistry; laboratory test; meta analysis (topic); mismatch repair; Muir Torre syndrome; multicenter study (topic); mutational analysis; oncogene; ovary carcinoma; polymerase chain reaction; PTEN gene; Review; risk assessment; Colorectal Neoplasms, Hereditary Nonpolyposis; Endometrial Neoplasms; Hamartoma Syndrome, Multiple; Muir-Torre Syndrome; pathology; DNA Mismatch Repair; Female; Humans; Risk Assessment
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/183610
• المؤسسة: National University of Singapore

10.1155/2015/219012