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The New England Journal of Medicine|August 15, 2014
Genotype-phenotype correlation--promiscuity in the era of next-generation sequencingJames T Lu, Philippe M Campeau, Brendan H LeeGenome Biology|March 2, 2012
Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphismsJames T Lu, Yi Wang, Richard A Gibbs, et al.Clinical Pharmacology and Therapeutics|April 30, 2021
Comprehensive Allele Genotyping in Critical Pharmacogenes Reduces Residual Clinical Risk in Diverse PopulationsShishi Luo, Ruomu Jiang, Joseph J Grzymski, et al.Biomaterials|December 13, 2006
Thin collagen film scaffolds for retinal epithelial cell cultureJames T Lu, Christina J Lee, Stacey F Bent, et al.Frontiers in Genetics|May 16, 2022
Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health RecordGai Elhanan, Daniel Kiser, Iva Neveux, et al.The Journal of Molecular Diagnostics : JMD|November 20, 2018
Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic TestingJames T Lu, Matthew Ferber, Jill Hagenkord, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 16, 2013
Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM5 geneMonica Grover, Philippe M Campeau, Caressa Dee Lietman, et al.Frontiers in Genetics|March 25, 2021
Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada PopulationRobert W Read, Karen A Schlauch, Vincent C Lombardi, et al.Human Mutation|June 21, 2012
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanismsPhilippe M Campeau, James T Lu, Brian C Dawson, et al.Molecular Genetics and Metabolism Reports|July 15, 2014
Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasiaChaya Murali, James T Lu, Mahim Jain, et al.Pageof 4