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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.
Authors van Vliet CM, Dowty JG, van Vliet JL, et al. Citation Hum Mutat. 2011 Feb;32(2):207-12. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21120946/ PMCID PMC3228833
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.
Authors Ward CJ, Wu Y, Johnson RA, et al. Citation Hum Genet. 2011 Mar;129(3):345-9. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21274727/ PMCID PMC3102497
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.
Authors Win AK, Cleary SP, Dowty JG, et al. Citation Int J Cancer. 2011 Nov 1;129(9):2256-62. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21171015/ PMCID PMC3291738
Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.
Authors Win AK, Dowty JG, Antill YC, et al. Citation Obstet Gynecol. 2011 Apr;117(4):899-905. PubMedLink https://pubmed.ncbi.nlm.nih.gov/21422863/ PMCID PMC3084323