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CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 21, 2015
A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case seriesIsabelle Rousseau-Nepton, Minoru Okubo, Rosemarie Grabs, et al.
BMC Endocrine Disorders|November 12, 2021
Causal variants in Maturity Onset Diabetes of the Young (MODY) - A systematic reviewIbrar Rafique, Asif Mir, Muhammad Arif Nadeem Saqib, et al.
Metabolism: Clinical and Experimental|February 1, 2022
Mendelian randomization study of obesity and type 2 diabetes in hospitalized COVID-19 patientsHui-Qi Qu, Jingchun Qu, Joseph Glessner, et al.
Journal of Human Genetics|August 28, 2019
Application of ACMG criteria to classify variants in the human gene mutation databaseHui-Qi Qu, Xiang Wang, Lifeng Tian, et al.
Annals of Neurology|January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic toolChee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Annals of Human Genetics|June 12, 2012
Familial clustering strongly suggests that the phenotypic variation of the 8344 A>G lys mitochondrial tRNA mutation is encoded in cisKyriakos Kazakos, Kalliopi Kotsa, Maria Yavropoulou, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|February 19, 2011
Molecular immunity to mycobacteria: knowledge from the mutation and phenotype spectrum analysis of Mendelian susceptibility to mycobacterial diseasesHui-Qi Qu, Susan P Fisher-Hoch, Joseph B McCormick
Journal of Human Genetics|December 24, 2010
Knowledge gaining by human genetic studies on tuberculosis susceptibilityHui-Qi Qu, Susan P Fisher-Hoch, Joseph B McCormick
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