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Journal 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 ButlerJournal of Neuroscience Research|April 29, 2008
Interactive roles of fibroblast growth factor 2 and neurotrophin 3 in the sequence of migration, process outgrowth, and axonal differentiation of mouse cochlear ganglion cellsWaheeda A Hossain, Chrystal D'Sa, D Kent MorestJournal of Neurobiology|May 5, 2006
Site-specific interactions of neurotrophin-3 and fibroblast growth factor (FGF2) in the embryonic development of the mouse cochlear nucleusWaheeda A Hossain, Chrystal D'Sa, D Kent MorestGenes|March 29, 2023
The Autism Spectrum: Behavioral, Psychiatric and Genetic AssociationsAnn Genovese, Merlin G ButlerEuropean 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 ButlerPageof 24