Showing results (181-190 of 275) with videos related to

Sort By:
Pageof 28
Journal of Aggression, Maltreatment & Trauma|December 7, 2020
Relationship Between Body Habitus and Aggression Subtypes Among Healthy Young Adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Steven G McNulty, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
X-chromosome inactivation patterns in females with Prader-Willi syndromeMerlin G Butler, Mariana F Theodoro, Douglas C Bittel, et al.
American Journal of Medical Genetics. Part A|December 18, 2018
Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomesRanim Mahmoud, Preeti Singh, Lan Weiss, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history studyMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.
Research in Developmental Disabilities|July 10, 2002
The role of residential homelikeness in promoting community participation by adults with mental retardationMark Egli, Irene Feurer, Todd Roper, et al.
Physical Chemistry Chemical Physics : PCCP|September 20, 2018
Tuning the photoreactivity of Z-hexatriene photoswitches by substituents - a non-adiabatic molecular dynamics studyEnrico Tapavicza, Travis Thompson, Kenneth Redd, et al.
Cytogenetic and Genome Research|November 29, 2016
Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3)Vy Dang, Abhilasha Surampalli, Ann M Manzardo, et al.
International Journal of Molecular Sciences|December 2, 2020
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum DisorderOlivia J Veatch, Merlin G Butler, Sarah H Elsea, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|February 7, 2017
FAMILIAL LARYNGEAL WEB IN THREE GENERATIONS WITH PROBABLE AUTOSOMAL DOMINANT TRANSMISSIONStephen M Strakowski, Merlin G Butler, James W Cheek, et al.
Pageof 28