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European Journal of Medical Genetics|November 29, 2019
Genetic variants in DGAT1 cause diverse clinical presentations of malnutrition through a specific molecular mechanismAditi Gupta, Nikita R Dsouza, Yuri A Zarate, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
Clinical and Translational Science|July 10, 2026
Machine Learning With Genetic and Clinical Data to Predict Ischemic Outcomes After PCICaroline W Grant, Brenden S Ingraham, Ryan J Lennon, et al.
Plos Neglected Tropical Diseases|September 9, 2016
Bacillus cereus Biovar Anthracis Causing Anthrax in Sub-Saharan Africa-Chromosomal Monophyly and Broad Geographic DistributionKym S Antonation, Kim Grützmacher, Susann Dupke, et al.
Journal of Neuropathology and Experimental Neurology|April 17, 2019
X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct DementiaPatrick R Blackburn, Wen-Lang Lin, David A Miller, et al.
Plos One|January 16, 2007
Genome-wide reverse genetics framework to identify novel functions of the vertebrate secretomeMichael A Pickart, Eric W Klee, Aubrey L Nielsen, et al.
Cancer Immunology Research|November 24, 2020
KIR3DL3 Is an Inhibitory Receptor for HHLA2 that Mediates an Alternative Immunoinhibitory Pathway to PD1Rupal S Bhatt, Abdulla Berjis, Julie C Konge, et al.
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