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American Journal of Medical Genetics. Part A|February 17, 2007
Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndromeMerlin G Butler, Douglas C BittelGenes|September 27, 2025
PTEN Gene and Autism: Genetic Underpinnings and Neurodevelopmental ImpactsAnn C Genovese, Merlin G ButlerBrain Sciences|April 27, 2024
Behavioral and Psychiatric Disorders in Syndromic AutismAnn C Genovese, Merlin G ButlerWorld Journal of Medical Genetics|March 28, 2017
Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndromeCarolyn S Kaufman, Merlin G ButlerJournal of Pediatric Genetics|September 13, 2016
A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication SyndromeDevin M Cox, Merlin G ButlerMedical Anthropology Quarterly|October 4, 2016
Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness PatterningF John Meaney, Merlin G ButlerGenes|February 26, 2025
Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric AssociationsAnn C Genovese, Merlin G ButlerPerspectives on Medical Education|February 8, 2020
Impostorism in third-year medical students: an item analysis using the Clance impostor phenomenon scaleBeth Levant, Jennifer A Villwock, Ann M ManzardoMental Illness|April 23, 2019
Repetitive transcranial magnetic stimulation (rTMS) using different TMS instruments for major depressive disorder at a suburban tertiary clinicMaria Cristina Davila, Brianna Ely, Ann M ManzardoMental Illness|July 9, 2019
Time to remission analysis for major depressive disorder after repetitive transcranial magnetic stimulation (rTMS)Ann M Manzardo, Brianna Ely, Maria Cristina DavilaPageof 26