Figure 2From: Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models Family 1. Pedigree illustrating need for population-specific probabilities of being a MSH2 mutation carrier and the probability of developing CRC and EC in cancer-free individuals in Family 1 from our sample.Back to article page