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Advanced Biology|June 9, 2022
Syndromic and Nonsyndromic Obesity: Underlying Genetic Causes in HumansJessica Duis, Merlin G ButlerCurrent Issues in Molecular Biology|January 30, 2026
Integrated Genetic and Protein Mechanisms Underlying Glucagon-like Peptide-1 Receptor Agonists in Treating Diabetes Mellitus and Weight LossLucas Francis, Merlin G ButlerThe Endocrinologist|August 30, 2016
Prader-Willi Syndrome: Clinical and Genetic FindingsMerlin G Butler, Travis ThompsonJournal of Pediatric Genetics|May 8, 2019
Classic Ehlers-Danlos Syndrome in a Son and Father with a Heart Transplant Performed in the FatherPaushpala Sen, Merlin G ButlerJournal of Neuroscience Research|February 14, 2003
Intracellular fibroblast growth factor produces effects different from those of extracellular application on development of avian cochleovestibular ganglion cells in vitroMasako M Bilak, Waheeda A Hossain, D Kent MorestJournal of Medical Genetics|May 7, 2018
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort studyMerlin G Butler, Samantha N Hartin, Waheeda A Hossain, et al.Journal 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 ButlerInternational 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 ButlerPageof 24