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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.
International 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.
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.
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.
International Journal of Molecular Sciences|February 25, 2015
Pharmacogenetics informed decision making in adolescent psychiatric treatment: a clinical case reportTeri Smith, Susan Sharp, Ann M Manzardo, et al.
The Journal of Rare Disorders|January 15, 2019
STARTLE RESPONSE ANALYSIS OF FOOD-IMAGE PROCESSING IN PRADER-WILLI SYNDROMEAlex Gabrielli, Albert B Poje, Ann Manzardo, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|March 23, 2011
TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndromeElisabeth M Dykens, Elizabeth Roof, Douglas Bittel, et al.
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