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Current Opinion in Pediatrics|November 5, 2020
Imprinting disorders in humans: a reviewMerlin G ButlerProgress in Molecular Biology and Translational Science|June 12, 2016
Single Gene and Syndromic Causes of Obesity: Illustrative ExamplesMerlin G ButlerTransactions of the Nebraska Academy of Sciences and Affiliated Societies|May 23, 2017
Sister Chromatid Exchanges in A Male With A Y/Y TranslocationMerlin G ButlerJournal of Pediatric Genetics|February 21, 2022
Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based ReviewMerlin G ButlerPrenatal Diagnosis|August 19, 2016
Benefits and limitations of prenatal screening for Prader-Willi syndromeMerlin G ButlerClinical Pediatrics|February 5, 2016
Growth Charts for Prader-Willi Syndrome During Growth Hormone TreatmentMerlin G Butler, Jaehoon Lee, Devin M Cox, et al.Substance Abuse|April 2, 2021
Covid19 impact screening of patients undergoing medication treatment for opioid use disorderAnn M Manzardo, Roopa SethiAlcoholism, Clinical and Experimental Research|August 26, 2006
A theoretical argument for inherited thiamine insensitivity as one possible biological cause of familial alcoholismAnn M Manzardo, Elizabeth C PenickEuropean Journal of Medical Genetics|September 24, 2016
Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defectsMaaz Hassan, Merlin G ButlerFrontiers in Pediatrics|June 2, 2020
Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and ApproachesMerlin G Butler, Jessica DuisPageof 26