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Journal 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 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 ButlerGenes|March 29, 2023
The Autism Spectrum: Behavioral, Psychiatric and Genetic AssociationsAnn Genovese, Merlin G ButlerPageof 28