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Journal of Neurodevelopmental Disorders|June 13, 2018
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigreesMarc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, et al.Journal of the American Heart Association|July 31, 2014
Remote ischemic preconditioning in children undergoing cardiac surgery with cardiopulmonary bypass: a single-center double-blinded randomized trialBrian W McCrindle, Nadia A Clarizia, Svetlana Khaikin, et al.The Cochrane Database of Systematic Reviews|September 4, 2024
Cardiovascular training versus resistance training for fatigue in people with cancerAnnika Oeser, Sarah Messer, Carina Wagner, et al.The Cochrane Database of Systematic Reviews|November 28, 2024
Resistance training for fatigue in people with cancerMoritz Ernst, Carina Wagner, Annika Oeser, et al.European Journal of Human Genetics : EJHG|March 19, 2022
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomaliesMiriam S Reuter, Michael Zech, Maja Hempel, et al.The Cochrane Database of Systematic Reviews|February 20, 2025
Cardiovascular training for fatigue in people with cancerCarina Wagner, Moritz Ernst, Nora Cryns, et al.European Journal of Human Genetics : EJHG|June 26, 2014
Prenatal growth restriction, retinal dystrophy, diabetes insipidus and white matter disease: expanding the spectrum of PRPS1-related disordersAlmundher Al-Maawali, Lucie Dupuis, Susan Blaser, et al.Molecular Psychiatry|November 26, 2014
The phenotypic manifestations of rare genic CNVs in autism spectrum disorderA K Merikangas, R Segurado, E A Heron, et al.Neurogenetics|March 20, 2014
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian familiesGerald Egger, Katharina M Roetzer, Abdul Noor, et al.Neurology|February 21, 2014
Peroxisomal D-bifunctional protein deficiency: three adults diagnosed by whole-exome sequencingMatthew A Lines, Rebekah Jobling, Lauren Brady, et al.Pageof 88