Showing results (121-130 of 246) with videos related to

Sort By:
Pageof 25
Gene|April 12, 2016
High-resolution chromosome ideogram representation of recognized genes for bipolar disorderLindsay N Douglas, Austen B McGuire, Ann M Manzardo, et al.
International Journal of Molecular Sciences|May 11, 2016
Morphometric Analysis of Recognized Genes for Autism Spectrum Disorders and Obesity in Relationship to the Distribution of Protein-Coding Genes on Human ChromosomesAusten B McGuire, Syed K Rafi, Ann M Manzardo, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Growth hormone receptor (GHR) gene polymorphism and Prader-Willi syndromeMerlin G Butler, Jennifer Roberts, Jena Hayes, et al.
American Journal of Medical Genetics|January 25, 2002
Oculoauriculofrontonasal syndrome (OAFNS) in a nine-month-old maleHolly A Ishmael, Michael L Begleiter, Elizabeth J Regier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality surveyMerlin G Butler, Ann M Manzardo, Janalee Heinemann, et al.
Pediatrics|March 3, 2004
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomyMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
Transfusion|March 15, 2012
Patient blood transfusion management: discharge hemoglobin level as a surrogate marker for red blood cell utilization appropriatenessJason Edwards, Chris Morrison, Maleeha Mohiuddin, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Increased plasma chemokine levels in children with Prader-Willi syndromeMerlin G Butler, Waheeda Hossain, Carlos Sulsona, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndromeSigan L Hartley, William E Maclean, Merlin G Butler, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disordersJacob Steinle, Waheeda A Hossain, Scott Lovell, et al.
Pageof 25