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Progress in Pediatric Cardiology|May 23, 2017
Gene expression in pediatric heart disease with emphasis on conotruncal defectsDouglas C Bittel, Nataliya Kibiryeva, James E O'Brien, et al.
American Journal of Medical Genetics. Part A|November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A reviewAdam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
International Journal of Molecular Sciences|February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A ReviewWaheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
CNS Neuroscience & Therapeutics|June 29, 2018
Tobacco and cannabis use in college students are predicted by sex-dimorphic interactions between MAOA genotype and child abusePaula J Fite, Shaquanna Brown, Waheeda Hossain, 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.
Journal of Mental Health Research in Intellectual Disabilities|February 7, 2017
Long-Term Aripiprazole in Youth With Developmental Disabilities Including AutismJessica A Hellings, Danna Boehm, Hung Wen Yeh, et al.
International Journal of Molecular Sciences|March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular InteractionsCaroline St Peter, Waheeda A Hossain, Scott Lovell, et al.
American Journal of Medical Genetics. Part A|January 20, 2007
Whole genome microarray analysis of gene expression in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Susan M Sell, et al.
Lipids in Health and Disease|March 18, 2011
Metabolic syndrome in South Asian immigrants: more than low HDL requiring aggressive managementSunita Dodani, Rebecca Henkhaus, Jo Wick, et al.
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