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Genes|September 28, 2021
Special Issue: Genetics of Prader-Willi SyndromeDavid E Godler, Merlin G ButlerJournal of Assisted Reproduction and Genetics|May 1, 2015
Androgen receptor (AR) gene CAG trinucleotide repeat length associated with body composition measures in non-syndromic obese, non-obese and Prader-Willi syndrome individualsMerlin G Butler, Ann M ManzardoAmerican 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 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 BhatnagarPageof 27