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Veterinary Parasitology|December 13, 2023
Understanding temporal and spatial distribution of intestinal nematodes of horses using faecal egg counts and DNA metabarcodingGhazanfar Abbas, Abdul Ghafar, Anne Beasley, et al.Molecular Genetics & Genomic Medicine|December 22, 2020
Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotypeLinda Z Rossetti, Mir Reza Bekheirnia, Andrea M Lewis, et al.BMJ Open|February 8, 2022
Development, deployment and evaluation of digitally enabled, remote, supported rehabilitation for people with long COVID-19 (Living With COVID-19 Recovery): protocol for a mixed-methods studyElizabeth Murray, Henry Goodfellow, Julia Bindman, et al.Preventive Veterinary Medicine|April 11, 2026
Simulation modelling as a tool to guide control strategies for foot and mouth disease in an endemic country: Nusa Tenggara Barat, Indonesia 2023-2024Y Yupiana, M A Stevenson, M Edwards, et al.Scientific Reports|December 1, 2022
Visual, spectral, and microchemical quantification of crystalline anomalies in otoliths of wild and cultured delta smeltLevi S Lewis, Jonathan L Huang, Malte Willmes, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 19, 2017
KIR3DL1/HLA-B Subtypes Govern Acute Myelogenous Leukemia Relapse After Hematopoietic Cell TransplantationJeanette E Boudreau, Fabio Giglio, Ted A Gooley, et al.European Journal of Haematology|September 6, 2023
Hyper-CVAD versus dose-adjusted EPOCH as initial treatment for adults with acute lymphoblastic leukemiaLucas C Zarling, Philip A Stevenson, Lorinda A Soma, et al.American Journal of Medical Genetics. Part A|June 22, 2019
Costello syndrome: Clinical phenotype, genotype, and management guidelinesKaren W Gripp, Lindsey A Morse, Marni Axelrad, et al.Plos One|January 28, 2014
Multiscale, converging defects of macro-porosity, microstructure and matrix mineralization impact long bone fragility in NF1Jirko Kühnisch, Jong Seto, Claudia Lange, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 7, 2015
Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failureSurabhi Mulchandani, Elizabeth J Bhoj, Minjie Luo, et al.Pageof 89