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International Journal of Molecular Sciences|March 11, 2023
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A ReviewMerlin G ButlerCurrent Opinion in Pediatrics|November 5, 2020
Imprinting disorders in humans: a reviewMerlin G ButlerProgress in Molecular Biology and Translational Science|June 12, 2016
Single Gene and Syndromic Causes of Obesity: Illustrative ExamplesMerlin G ButlerTransactions of the Nebraska Academy of Sciences and Affiliated Societies|May 23, 2017
Sister Chromatid Exchanges in A Male With A Y/Y TranslocationMerlin G ButlerJournal of Pediatric Genetics|February 21, 2022
Prolapsed Rectum and Risk Factors in Prader-Willi Syndrome: A Case-Based ReviewMerlin G ButlerPrenatal Diagnosis|August 19, 2016
Benefits and limitations of prenatal screening for Prader-Willi syndromeMerlin G ButlerTransfusion|March 30, 2010
Regional registry of patient alloantibodies: first-year experienceVicki Schwickerath, Mary Kowalski, Jay E MenitoveEuropean 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 ButlerPageof 25