Impact of colon cancer screening on family history phenotype.

Authors Newcomb PA, Savu A, Phipps AI, et al.
Citation Epidemiology. 2012 Mar;23(2):308-10.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22252410/
PMCID PMC3299289

Determining the frequency of de novo germline mutations in DNA mismatch repair genes.

Funded by the National Cancer
Institute (NCI), U01 CA167551, NIH USA