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BMC Medical Genetics|January 21, 2011
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndromeAdela Castillejo, Carla Guarinos, Ana Martinez-Canto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2014
Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancerClara Esteban-Jurado, Maria Vila-Casadesús, Pilar Garre, et al.
BMC Genomics|January 29, 2013
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12Ceres Fernandez-Rozadilla, Jean-Baptiste Cazier, Ian P Tomlinson, et al.
Carcinogenesis|May 29, 2013
Genetic susceptibility variants associated with colorectal cancer prognosisAnna Abulí, Juan José Lozano, María Rodríguez-Soler, et al.
The Pharmacogenomics Journal|May 3, 2019
Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn's diseaseAdrià Aterido, Núria Palau, Eugeni Domènech, et al.
Carcinogenesis|November 20, 2012
BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern European populationsCeres Fernandez-Rozadilla, Claire Palles, Luis Carvajal-Carmona, et al.
Preventive Medicine|January 30, 2017
Relationship between drugs affecting the renin-angiotensin system and colorectal cancer: The MCC-Spain studyTrinidad Dierssen-Sotos, Inés Gómez-Acebo, Camilo Palazuelos, et al.
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