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2. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report

3. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer

5. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

6. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas

8. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene

9. High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

11. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)

14. Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis

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