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Scientific Reports|September 21, 2019
Marked variation in heritability estimates of left ventricular mass depending on modality of measurementRichard M Nethononda, Kathryn A McGurk, Polly Whitworth, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2018
A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE)Hiba Alblooshi, Habiba Al Safar, Holly F Fisher, et al.The Journal of Allergy and Clinical Immunology|March 4, 2008
Filaggrin null mutations and childhood atopic eczema: a population-based case-control studySara J Brown, Caroline L Relton, Haihui Liao, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 11, 2021
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal PopulationSarra E Jamieson, Michaela Fakiola, Dave Tang, et al.Nature Genetics|August 1, 1993
Polygenic control of autoimmune diabetes in nonobese diabetic miceS Ghosh, S M Palmer, N R Rodrigues, et al.BMC Genetics|May 12, 2005
Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humansClive J Petry, Ken K Ong, Bryan J Barratt, et al.Plos One|June 5, 2015
Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility LocusAnna L Mitchell, Anette Bøe Wolff, Katie MacArthur, et al.Annals of the Rheumatic Diseases|August 1, 2020
Investigation of genetically regulated gene expression and response to treatment in rheumatoid arthritis highlights an association between IL18RAP expression and treatment responseSvetlana Cherlin, Myles J Lewis, Darren Plant, et al.Annals of Clinical and Translational Neurology|March 22, 2018
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factorsSarah J Pickett, John P Grady, Yi Shiau Ng, et al.The Journal of Clinical Endocrinology and Metabolism|September 21, 2006
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) geneHelen Imrie, Marie Freel, Bongani M Mayosi, et al.Pageof 27