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Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Homozygosity for aCHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype
Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort
A review of the genetic background and tumour profiling in familial colorectal cancer
