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Familial Cancer|May 5, 2020
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicingTamara Alejandra Piñero, Omar Soukarieh, Marion Rolain, et al.Familial Cancer|May 8, 2004
Intron 4 mutation in APC gene results in splice defect and attenuated FAP phenotypeDeborah W Neklason, Cindy H Solomon, Amy L Dalton, et al.Familial Cancer|May 8, 2004
Patients' and professionals' opinions of services for people at an increased risk of colorectal cancer: an exploratory qualitative studyTamar Stermer, Shirley Hodgson, Fred Kavalier, et al.Familial Cancer|September 2, 2004
Promoter hypermethylation frequency and BRAF mutations distinguish hereditary non-polyposis colon cancer from sporadic MSI-H colon cancerA McGivern, C V A Wynter, V L J Whitehall, et al.Familial Cancer|November 2, 2004
Cancer in Jews: introduction and overviewHenry T Lynch, Wendy S Rubinstein, Gershon Y LockerFamilial Cancer|November 2, 2004
The Jewish people: their ethnic history, genetic disorders and specific cancer susceptibilityInbal Kedar-Barnes, Paul RozenFamilial Cancer|September 16, 2022
Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylationVincent M T de Jong, Roelof Pruntel, Tessa G Steenbruggen, et al.Familial Cancer|November 24, 2021
Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancerJames M Chan, Mark Clendenning, Sharelle Joseland, et al.Pageof 152