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Genes|March 4, 2020
Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi SyndromeHarold J P van Bosse, Merlin G ButlerCurrent Opinion in Psychiatry|January 13, 2025
Genetics of Prader-Willi and Angelman syndromes: 2024 updateDavid E Godler, Deepan Singh, Merlin G ButlerGenomics|September 5, 2006
X chromosome gene expression in human tissues: male and female comparisonsZohreh Talebizadeh, Stephen D Simon, Merlin G ButlerPediatrics|September 20, 2006
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Merlin G ButlerCurrent Genomics|February 2, 2012
Genetics and mitochondrial abnormalities in autism spectrum disorders: a reviewSukhbir Dhillon, Jessica A Hellings, Merlin G ButlerAutism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autismZohreh Talebizadeh, Merlin G Butler, Mariana F TheodoroJournal of Environmental Science and Health. Part A, Environmental Science and Engineering|November 8, 2016
CHROMOSOME BREAKAGE AND SISTER CHROMATID EXCHANGE ANALYSIS IN COMPUTER OPERATORSMerlin G Butler, Jennifer Yost, Bonnie B JenkinsCytogenetic and Genome Research|November 24, 2016
Deletion of TOP3B Is Associated with Cognitive Impairment and Facial DysmorphismCarolyn S Kaufman, Ann Genovese, Merlin G ButlerJournal of Pediatric Endocrinology & Metabolism : JPEM|October 28, 2004
Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndromeMerlin G Butler, Douglas C Bittel, Zohreh TalebizadehGenetic Testing|February 26, 2008
Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalitiesDouglas C Bittel, Nataliya Kibiryeva, Merlin G ButlerPageof 26