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Frontiers in Pediatrics|April 8, 2021
Genetic and Non-genetic Workup for Pediatric Congenital Hearing LossRyan Belcher, Frank Virgin, Jessica Duis, et al.American Journal of Medical Genetics. Part A|February 13, 2008
Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndromeMerlin G Butler, William Fischer, Nataliya Kibiryeva, et al.Genes|February 25, 2022
Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic TestingMerlin G Butler, Daniel Moreno-De-Luca, Antonio M PersicoJournal of Pediatric Genetics|September 13, 2016
The 7q11.23 Microduplication Syndrome: A Clinical Report with Review of LiteratureElham Abbas, Devin M Cox, Teri Smith, et al.PJE. Peabody Journal of Education|September 6, 2016
Prader-Willi Syndrome: Genetics and BehaviorTravis Thompson, Merlin G Butler, William E MacLean, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 11, 2002
Newborn with anophthalmia and features of Fryns syndromeDiane M Pierson, Antonio Subtil, Eugenio Taboada, et al.Genes|December 30, 2025
Barriers, Limitations, and Experiences with Clinical Trials-Treatment in Rare Diseases with Prader-Willi Syndrome as an ExampleMerlin G Butler, Spencer Silvey, Harold J P van BosseInternational Journal of Molecular Sciences|January 21, 2023
Chromosomal Microarray Study in Prader-Willi SyndromeMerlin G Butler, Waheeda A Hossain, Neil Cowen, et al.American Journal of Medical Genetics. Part A|November 13, 2021
PHIP gene variants with protein modeling, interactions, and clinical phenotypesJordan Dietrich, Scott Lovell, Olivia J Veatch, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2006
C-reactive protein levels in subjects with Prader-Willi syndrome and obesityMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.Pageof 27