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European Journal of Medical Genetics|September 24, 2016
Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defectsMaaz Hassan, Merlin G ButlerFrontiers in Pediatrics|June 2, 2020
Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and ApproachesMerlin G Butler, Jessica DuisJournal of Pediatric Genetics|July 28, 2020
22q11.2 Microduplications: Two Clinical Reports Compared with Similar Cases from the LiteratureAderonke Oyetunji, Merlin G ButlerArchives of Gynecology and Obstetrics|June 29, 2019
Ehlers-Danlos syndrome and other heritable connective tissue disorders that impact pregnancies can be detected using next-generation DNA sequencingKrystal VanderJagt, Merlin G ButlerInternational Journal of Molecular Sciences|July 8, 2020
Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD)Ann Genovese, Merlin G ButlerAdvanced 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 ButlerJournal 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 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 ButlerPageof 28