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11. Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC. Di Fiore F; Charbonnier F; Martin C; Frerot S; Olschwang S; Wang Q; Boisson C; Buisine MP; Nilbert M; Lindblom A; Frebourg T J Med Genet; 2004 Jan; 41(1):18-20. PubMed ID: 14729822 [No Abstract] [Full Text] [Related]
13. DNA mismatch repair and cancer. Peltomäki P Mutat Res; 2001 Mar; 488(1):77-85. PubMed ID: 11223406 [TBL] [Abstract][Full Text] [Related]
14. Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes. Wang Y; Friedl W; Lamberti C; Jungck M; Mathiak M; Pagenstecher C; Propping P; Mangold E Int J Cancer; 2003 Feb; 103(5):636-41. PubMed ID: 12494471 [TBL] [Abstract][Full Text] [Related]
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17. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene. Shin KH; Shin JH; Kim JH; Park JG Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355 [TBL] [Abstract][Full Text] [Related]
18. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. Lindor NM; Rabe K; Petersen GM; Haile R; Casey G; Baron J; Gallinger S; Bapat B; Aronson M; Hopper J; Jass J; LeMarchand L; Grove J; Potter J; Newcomb P; Terdiman JP; Conrad P; Moslein G; Goldberg R; Ziogas A; Anton-Culver H; de Andrade M; Siegmund K; Thibodeau SN; Boardman LA; Seminara D JAMA; 2005 Apr; 293(16):1979-85. PubMed ID: 15855431 [TBL] [Abstract][Full Text] [Related]
19. Molecular screening for the Lynch syndrome--better than family history? Lynch HT; Lynch PM N Engl J Med; 2005 May; 352(18):1920-2. PubMed ID: 15872208 [No Abstract] [Full Text] [Related]