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Frontiers in Genetics|December 17, 2020
Pharmacodynamic Gene Testing in Prader-Willi SyndromeJanice Forster, Jessica Duis, Merlin G ButlerGenes|January 27, 2021
Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi SyndromeJanice Forster, Jessica Duis, Merlin G ButlerFrontiers in Pediatrics|June 2, 2020
Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and ApproachesMerlin G Butler, Jessica DuisAdvanced Biology|June 9, 2022
Syndromic and Nonsyndromic Obesity: Underlying Genetic Causes in HumansJessica Duis, Merlin G ButlerJournal of Pediatric Endocrinology & Metabolism : JPEM|January 4, 2003
Imprinting disorders: non-Mendelian mechanisms affecting growthMerlin G ButlerJournal. Tennessee Academy of Science|February 7, 2017
FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDYMerlin G ButlerCurrent Genomics|November 2, 2011
Prader-Willi Syndrome: Obesity due to Genomic ImprintingMerlin G ButlerJournal of Assisted Reproduction and Genetics|October 22, 2009
Genomic imprinting disorders in humans: a mini-reviewMerlin G ButlerInternational Journal of Molecular Sciences|February 13, 2026
Clinical Presentation, Genetics, and Laboratory Testing with Integrated Genetic Analysis of Molecular Mechanisms in Prader-Willi and Angelman Syndromes: A ReviewMerlin G ButlerLe Journal Medical Libanais. the Lebanese Medical Journal|April 6, 2011
Genetics of hypertension. Current statusMerlin G ButlerPageof 27