Showing results (1851-1860 of 2,010) with videos related to
Sort By:
Pageof 201
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Symptom-led staging for primary progressive aphasiaChris Jd Hardy, Cathleen Taylor-Rubin, Beatrice Taylor, et al.NPJ Genomic Medicine|February 27, 2025
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric diseaseKatherine B Howell, Susan M White, Amy McTague, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 14, 2023
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium studyPatrick M Sleiman, Hui-Qi Qu, John J Connolly, et al.Bioorganic & Medicinal Chemistry Letters|December 20, 2017
Dihydrobenzisoxazole-4-one compounds are novel selective inhibitors of aldosterone synthase (CYP11B2) with in vivo activityKenneth Meyers, Derek A Cogan, Jennifer Burke, et al.Journal of Medical Genetics|March 31, 2018
Chitayat-Hall and Schaaf-Yang syndromes:a common aetiology: expanding the phenotype of MAGEL2-related disordersRebekah Jobling, Dimitri James Stavropoulos, Christian R Marshall, et al.American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.Global Change Biology|January 26, 2024
Global dominance of lianas over trees is driven by forest disturbance, climate and topographyAlain Senghor K Ngute, David S Schoeman, Marion Pfeifer, et al.Human Mutation|February 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discoveryHannah G Driver, Taila Hartley, E Magda Price, et al.Frontiers in Molecular Neuroscience|March 3, 2020
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export FactorRaman Kumar, Elizabeth Palmer, Alison E Gardner, et al.JAMA Network Open|September 22, 2020
Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical ComplexityGregory Costain, Susan Walker, Maria Marano, et al.Pageof 201