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International Journal of Molecular Sciences|May 10, 2020
The 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental PhenotypesSyed K Rafi, Merlin G ButlerExpert Reviews in Molecular Medicine|July 26, 2005
Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biologyDouglas C Bittel, Merlin G ButlerInternational Journal of Molecular Sciences|February 18, 2015
The 15q11.2 BP1-BP2 microdeletion syndrome: a reviewDevin M Cox, Merlin G ButlerClinical Dysmorphology|February 26, 2015
A clinical case report and literature review of the 3q29 microdeletion syndromeDevin M Cox, Merlin G ButlerCytogenetic and Genome Research|April 15, 2015
Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal AbnormalitiesDevin M Cox, Merlin G ButlerAmerican Journal of Medical Genetics. Part A|August 21, 2012
Development and implementation of electronic growth charts for infants with Prader-Willi syndromeS Trent Rosenbloom, Merlin G ButlerJournal of Assisted Reproduction and Genetics|May 28, 2011
Umbilical cord blood banking: an updateMerlin G Butler, Jay E MenitoveJournal of Pediatric Genetics|October 14, 2014
Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndromeAdria M Jerkovich, Merlin G ButlerClinical Genetics|September 18, 2024
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A reviewAmin J Barakat, Merlin G ButlerFrontiers in Genetics|June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databasesWaheeda A Hossain, Merlin G ButlerPageof 27