Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors-Reference-Cited by-同舟云学术

Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

Published:2014-03 Issue:3 Volume:146 Page:643-646.e8
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Mensenkamp Arjen R.,Vogelaar Ingrid P.,van Zelst–Stams Wendy A.G.,Goossens Monique,Ouchene Hicham,Hendriks–Cornelissen Sandra J.B.,Kwint Michael P.,Hoogerbrugge Nicoline,Nagtegaal Iris D.,Ligtenberg Marjolijn J.L.

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference41 articles.

1. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

2. Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

3. The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome

4. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

5. Frequency of loss ofhMLH1 expression in colorectal carcinoma increases with advancing age

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