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Germline EPHB2 receptor variants in familial colorectal cancer.
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Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
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The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
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Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening.
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Pathological features of colorectal carcinomas in MYH-associated polyposis.
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Efficient p-value estimation in massively parallel testing problems.
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