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The American Journal of Pathology|April 23, 2003
Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancersSarah E R Halford, Andrew J Rowan, Lara Lipton, et al.
Breast Cancer Research : BCR|October 29, 2003
Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA)Carmel Apicella, Lesley Andrews, Shirley V Hodgson, et al.
Human Molecular Genetics|March 24, 2022
Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau diseaseAvgi Andreou, Bryndis Yngvadottir, Laia Bassaganyas, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 17, 2008
Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCNEmma R Woodward, Christopher Ricketts, Pip Killick, et al.
Clinical Endocrinology|February 21, 2004
Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibilityDewi Astuti, Niki Hart-Holden, Farida Latif, et al.
The New England Journal of Medicine|February 28, 2003
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYHOliver M Sieber, Lara Lipton, Michael Crabtree, et al.
Human Molecular Genetics|March 27, 2013
DNA polymerase ε and δ exonuclease domain mutations in endometrial cancerDavid N Church, Sarah E W Briggs, Claire Palles, et al.
Cancer Research|November 25, 2003
Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathwayLara Lipton, Sarah E Halford, Victoria Johnson, et al.
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