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Journal 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 ButlerInternational Journal of Molecular Sciences|June 19, 2019
Magnesium Supplement and the 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: A Potential Treatment?Merlin G ButlerInternational Journal of Molecular Sciences|March 11, 2023
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A ReviewMerlin G ButlerCurrent 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 ButlerPageof 24