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Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).
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Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated lynch syndrome cases.
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Calcium and vitamin D and risk of colorectal cancer: results from a large population-based case-control study in Newfoundland and Labrador and Ontario.
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Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
Authors Tomlinson IP, Carvajal-Carmona LG, Dobbins SE, et al. Citation PLoS Genet. 2011 Jun;7(6):e1002105. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21655089/ PMCID PMC3107194
Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes.
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Cancer: Lynch syndrome–how should colorectal cancer be managed?
Authors Vasen HF, de Vos tot Nederveen Cappel WH. Citation Nat Rev Gastroenterol Hepatol. 2011 Apr;8(4):184-6. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21460875/ PMCID NA
Germline PKHD1 mutations are protective against colorectal cancer.
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Lynch syndrome: barriers to and facilitators of screening and disease management.
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Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.
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