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Total 1 results found since Jan 2013.
First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome
In this study, we confirmed that MSH2 , MLH1, and MSH6 contribute to CRC susceptibility. This work represents the implementation of a diagnostic algorithm for the identification of Lynch syndrome patients in Algerian families.
Source: Familial Cancer - July 27, 2016 Category: Cancer & Oncology Source Type: research
