Showing results (141-150 of 275) with videos related to

Sort By:
Pageof 28
Genomics|December 21, 2004
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPDDouglas C Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, et al.
Drug and Alcohol Dependence|April 25, 2015
Change in psychiatric symptomatology after benfotiamine treatment in males is related to lifetime alcoholism severityAnn M Manzardo, Tiffany Pendleton, Albert Poje, et al.
Intellectual and Developmental Disabilities|August 6, 2016
"My Voice Counts, Too": Voting Participation Among Individuals With Intellectual DisabilityMartin Agran, William E MacLean, Katherine Anne Arden Kitchen
Genes|July 24, 2019
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire SurveyAnn M Manzardo, Janalee Heinemann, Barbara McManus, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2022
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndromeMoris A Angulo, Merlin G Butler, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysisDouglas C Bittel, Nataliya Kibiryeva, Majed Dasouki, et al.
Progress in Pediatric Cardiology|May 23, 2017
Gene expression in pediatric heart disease with emphasis on conotruncal defectsDouglas C Bittel, Nataliya Kibiryeva, James E O'Brien, et al.
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.
International Journal of Molecular Sciences|July 21, 2019
High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA StudiesSyed K Rafi, Alberto Fernández-Jaén, Sara Álvarez, 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.
Pageof 28