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The Journal of Pediatrics|June 23, 2019
Damaging Variants in Proangiogenic Genes Impair Growth in Fetuses with Cardiac DefectsMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.JAMA Psychiatry|March 17, 2016
Structural Brain Abnormalities in Youth With Psychosis Spectrum SymptomsTheodore D Satterthwaite, Daniel H Wolf, Monica E Calkins, et al.Neuroimage|August 8, 2013
Neuroimaging of the Philadelphia neurodevelopmental cohortTheodore D Satterthwaite, Mark A Elliott, Kosha Ruparel, et al.Journal of Neurology|November 1, 2014
Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutationsCecilia Mancini, Stefano Nassani, Yiran Guo, et al.British Journal of Haematology|October 15, 2013
Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changesDaria V Babushok, Hongbo M Xie, Jacquelyn J Roth, et al.Data in Brief|August 28, 2019
Effect of parental origin of damaging variants in pro-angiogenic genes on fetal growth in patients with congenital heart defects: Data and analysesMark W Russell, Julie S Moldenhauer, Jack Rychik, et al.European Journal of Human Genetics : EJHG|January 28, 2016
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionIvana Matera, Marta Rusmini, Yiran Guo, et al.Gene|October 11, 2025
Genome-wide association study and HLA genotyping for beryllium disease susceptibility in a European descent populationShu-Yi Liao, Tasha E Fingerlin, Sean Jacobson, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 10, 2017
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal SitesAlessandra Chesi, Jonathan A Mitchell, Heidi J Kalkwarf, et al.Orphanet Journal of Rare Diseases|April 24, 2020
Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndromeYueheng Wu, Yu Xia, Ping Li, et al.Pageof 91