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Cancer Biology & Medicine|May 5, 2016
Current practices and guidelines for clinical next-generation sequencing oncology testingSamuel P StromMethods in Molecular Biology (Clifton, N.J.)|December 13, 2018
Fundamentals of RNA Analysis on Biobanked SpecimensSamuel P StromMolecular Vision|May 21, 2013
Evaluation of autosomal dominant retinal dystrophy genes in an unaffected cohort suggests rare or private missense variants may often be benignSamuel P Strom, Michael B GorinAnnals of the New York Academy of Sciences|August 8, 2015
Clinical exome sequencing in neurogenetic and neuropsychiatric disordersBrent L Fogel, Hane Lee, Samuel P Strom, et al.American Journal of Medical Genetics. Part A|September 9, 2018
Geleophysic dysplasia: 48 year clinical update with emphasis on cardiac careJanet M Legare, Peggy Modaff, Samuel P Strom, et al.HGG Advances|March 15, 2021
Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopiaAbidemi Adegbola, Richard Lutz, Elina Nikkola, et al.American Journal of Medical Genetics. Part A|July 29, 2022
Next-generation sequencing and analysis of consecutive patients referred for connective tissue disordersJacob Steinle, Waheeda A Hossain, Olivia J Veatch, et al.BMC Medical Genetics|January 22, 2014
Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophyMaria Carolina Ortube, Samuel P Strom, Stanley F Nelson, et al.Plos One|January 5, 2010
Disease gene characterization through large-scale co-expression analysisAllen Day, Jun Dong, Vincent A Funari, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 11, 2014
Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratorySamuel P Strom, Hane Lee, Kingshuk Das, et al.Pageof 4