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Journal of Glaucoma|January 7, 2010
Lack of association of polymorphisms in elastin with pseudoexfoliation syndrome and glaucomaBao Jian Fan, Dayse R Figuieredo Sena, Louis R Pasquale, et al.Clinical Pharmacology and Therapeutics|June 29, 2000
Human beta2-adrenergic receptor polymorphisms: no association with essential hypertension in black or white AmericansH G Xie, C M Stein, R B Kim, et al.Human Molecular Genetics|April 18, 2000
Genome-wide scan for adult onset primary open angle glaucomaJ L Wiggs, R R Allingham, A Hossain, et al.Pharmacotherapy|June 24, 2016
A Self-Assessment Guide for Resident Teaching ExperiencesJanet P Engle, Amy M Franks, Emily Ashjian, et al.Genomics|August 1, 1988
Genetic linkage map of human chromosome 21R E Tanzi, J L Haines, P C Watkins, et al.Annals of Human Genetics|January 30, 1999
Comprehensive mutational analysis of the TSC1 gene: observations on frequency of mutation, associated features, and nonpenetranceJ Kwiatkowska, S Jozwiak, F Hall, et al.Science (New York, N.Y.)|August 13, 1993
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset familiesE H Corder, A M Saunders, W J Strittmatter, et al.AIDS (London, England)|August 17, 2005
Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group studyTodd Hulgan, David W Haas, Jonathan L Haines, et al.Journal of Medical Genetics|January 1, 1993
Exclusion of familial dysautonomia from more than 60% of the genomeA Blumenfeld, F B Axelrod, J A Trofatter, et al.Human Mutation|February 26, 2009
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10Xueying Liang, Michael Slifer, Eden R Martin, et al.Pageof 93