Showing results (141-150 of 246) with videos related to

Sort By:
Pageof 25
American Journal of Medical Genetics. Part A|November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A reviewAdam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
American Journal of Medical Genetics. Part A|May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controlsAnn M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
International Journal of Molecular Sciences|February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A ReviewWaheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
CNS Neuroscience & Therapeutics|June 29, 2018
Tobacco and cannabis use in college students are predicted by sex-dimorphic interactions between MAOA genotype and child abusePaula J Fite, Shaquanna Brown, Waheeda Hossain, et al.
American Journal of Medical Genetics. Part A|December 1, 2015
Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblingsLisa Johnson, Ann M Manzardo, Jennifer L Miller, et al.
American Journal of Medical Genetics. Part A|August 13, 2016
Higher plasma orexin a levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controlsAnn M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
American Journal of Medical Genetics. Part A|July 29, 2022
Next-generation sequencing and analysis of consecutive patients referred for connective tissue disordersJacob Steinle, Waheeda A Hossain, Olivia J Veatch, et al.
Journal of Mental Health Research in Intellectual Disabilities|February 7, 2017
Long-Term Aripiprazole in Youth With Developmental Disabilities Including AutismJessica A Hellings, Danna Boehm, Hung Wen Yeh, et al.
Genetics Research International|November 18, 2014
Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant BehaviorMerlin G Butler, Kelly Usrey, Jennifer L Roberts, et al.
Pageof 25