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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.Familial Cancer|October 12, 2022
A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variantMadeline Foley, Anu Sharma, Kinley Garfield, et al.Familial Cancer|June 10, 2011
The LKB1 complex-AMPK pathway: the tree that hides the forestMichaël Sebbagh, Sylviane Olschwang, Marie-Josée Santoni, et al.Familial Cancer|May 21, 2011
Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German familiesAngela Brieger, Knut Engels, Dieter Schaefer, et al.Pageof 151