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Plos One|March 22, 2016
Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen ConsortiumFaye L Norby, Samuel Adamsson Eryd, Maartje N Niemeijer, et al.
Clinical Genetics|July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorderStephanie Oates, Michael Absoud, Sushma Goyal, et al.
Journal of Cardiac Failure|May 9, 2015
Advanced (stage D) heart failure: a statement from the Heart Failure Society of America Guidelines CommitteeJames C Fang, Gregory A Ewald, Larry A Allen, et al.
Genetics in Medicine Open|November 1, 2024
Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testingJonathan Marquez, Jennifer N Cech, Cate R Paschal, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|December 27, 2024
Optimizing Ewing Sarcoma and Osteosarcoma Biopsy Acquisition: A Children's Oncology Group Bone Tumor Committee Consensus StatementMatthew S Dietz, Alyaa Al-Ibraheemi, Jessica L Davis, et al.
BMJ Open|February 13, 2021
Seroprevalence of antibodies to SARS-CoV-2 in healthcare workers: a cross-sectional studyJoseph E Ebinger, Gregory J Botwin, Christine M Albert, et al.
Cancer Discovery|October 19, 2022
Intraventricular B7-H3 CAR T Cells for Diffuse Intrinsic Pontine Glioma: Preliminary First-in-Human Bioactivity and SafetyNicholas A Vitanza, Ashley L Wilson, Wenjun Huang, et al.
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