Gynecologic Cancers in Lynch Syndrome/HNPCC
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics(clinical),Oncology,Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10689-005-1838-3.pdf
Reference29 articles.
1. Cancer risk in mutation carriers of DNA-mismatch-repair genes
2. Cancer risk associated with germline DNA mismatch repair gene mutations
3. Gynecological Tumors in Hereditary Nonpolyposis Colorectal Cancer: We Know They Are Common—Now What?
4. MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families
5. Impact of Gender and Parent of Origin on the Phenotypic Expression of Hereditary Nonpolyposis Colorectal Cancer in a Large Newfoundland Kindred With a Common MSH2 Mutation
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1. Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer;Familial Cancer;2023-06-21
2. Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General Population;Journal of Clinical Medicine;2022-06-27
3. Initial screening by immunohistochemistry is effective in universal screening for Lynch syndrome in endometrial cancer patients: a prospective observational study;Japanese Journal of Clinical Oncology;2022-04-18
4. EPM2AIP1 Immunohistochemistry can be Used as Surrogate Testing for MLH1 Promoter Methylation in Endometrial Cancer;American Journal of Surgical Pathology;2021-11-15
5. Predictive and Prognostic Value of Microsatellite Instability in Gynecologic Cancer (Endometrial and Ovarian);Cancers;2021-05-18
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