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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
<i>PTEN</i> 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 ButlerAmerican Journal of Medical Genetics. Part A|July 18, 2019
Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass indexMerlin G Butler, Naomi A Matthews, Nidhi Patel, et al.World Journal of Medical Genetics|March 28, 2017
Mutation in <i>TNXB</i> 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 ButlerAmerican Journal of Medical Genetics. Part A|October 3, 2022
Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findingsMerlin G Butler, Neil Cowen, Anish BhatnagarFrontiers in Genetics|December 17, 2020
Pharmacodynamic Gene Testing in Prader-Willi SyndromeJanice Forster, Jessica Duis, Merlin G ButlerPageof 28