Related Articles
Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients
Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer
The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC
Novel MSH2 splice-site mutation in a young patient with Lynch syndrome
Real‑world outcome of universal screening for Lynch syndrome in Japanese patients with colorectal cancer highlights the importance of targeting patients with young‑onset disease