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The Lancet. Oncology|December 13, 2021
Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association studyEric Trépo, Stefano Caruso, Jie Yang, et al.Ebiomedicine|January 11, 2020
Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic studyAbderrahim Oussalah, Elise Jeannesson-Thivisol, Céline Chéry, et al.Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.Oncotarget|October 4, 2017
BRIP1 coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver diseaseAbderrahim Oussalah, Patrice Hodonou Avogbe, Erwan Guyot, et al.Journal of Medical Genetics|June 27, 2024
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patientsHortense Thomas, Tom Alix, Émeline Renard, et al.Pageof 9