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Thyroid : Official Journal of the American Thyroid Association|November 9, 2010
Analysis of immune regulatory genes' copy number variants in Graves' diseaseAmanda K Huber, Erlinda S Concepcion, Alisha Gandhi, et al.Frontiers in Endocrinology|March 26, 2016
Dissecting the Genetic Susceptibility to Graves' Disease in a Cohort of Patients of Italian OriginAngela Lombardi, Francesca Menconi, David Greenberg, et al.Springerplus|February 12, 2013
Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexesLeah C Kottyan, Jessica G Woo, Mehdi Keddache, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|March 26, 2013
Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing lossTheru A Sivakumaran, Ammar Husami, Diane Kissell, et al.Human Genetics|January 5, 2007
Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformationsLisa J Martin, Vijaya Ramachandran, Linda H Cripe, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 14, 2012
Genetically driven target tissue overexpression of CD40: a novel mechanism in autoimmune diseaseAmanda K Huber, Fred D Finkelman, Cheuk Wun Li, et al.Circulation. Cardiovascular Genetics|August 3, 2014
Whole exome sequencing for familial bicuspid aortic valve identifies putative variantsLisa J Martin, Valentina Pilipenko, Kenneth M Kaufman, et al.Archives of Otolaryngology--Head & Neck Surgery|August 20, 2003
Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United StatesLynne H Y Lim, John K Bradshaw, Yingshi Guo, et al.Neuroscience Letters|February 5, 2008
Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsyKatherine D Holland, Jennifer A Kearney, Tracy A Glauser, et al.Annals of Neurology|February 7, 2017
Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsyTracy A Glauser, Katherine Holland, Valerie P O'Brien, et al.Pageof 4