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Advances in Genomics and Genetics|February 24, 2015
Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromesMerlin G Butler, Kun Wang, Jan D Marshall, et al.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 ButlerLe Journal Medical Libanais. the Lebanese Medical Journal|April 6, 2011
Genetics of hypertension. Current statusMerlin G ButlerWorld Journal of Cardiology|September 4, 2020
Classic Ehlers-Danlos syndrome and cardiac transplantation - Is there a connection?Merlin 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 ButlerPageof 26