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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Möslein G, Fodde R. van der Klift H, et al. Among authors: fodde r. Genes Chromosomes Cancer. 2005 Oct;44(2):123-38. doi: 10.1002/gcc.20219. Genes Chromosomes Cancer. 2005. PMID: 15942939
CA repeat polymorphism within the MCC (mutated in colorectal cancer) gene.
van Leeuwen C, Tops C, Breukel C, van der Klift H, Deaven L, Fodde R, Khan PM. van Leeuwen C, et al. Among authors: fodde r. Nucleic Acids Res. 1991 Oct 25;19(20):5805. doi: 10.1093/nar/19.20.5805. Nucleic Acids Res. 1991. PMID: 1945868 Free PMC article. No abstract available.
DGGE polymorphism in intron 10 of MSH2, the HNPCC gene.
Wijnen J, Fodde R, Khan PM. Wijnen J, et al. Among authors: fodde r. Hum Mol Genet. 1994 Dec;3(12):2268. doi: 10.1093/hmg/3.12.2268-a. Hum Mol Genet. 1994. PMID: 7881445 No abstract available.
197 results