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Cureus|December 2, 2025
Frailty as a Predictor of Outcomes in OptiflowMatthew Mort, Alwin Raju, Naina MohanClinical Medicine (London, England)|September 11, 2021
Metabolic emergencies in pregnancyNaina Mohan, Anita BanerjeeThe Clinical Teacher|July 10, 2013
A Considerative Checklist to ensure safe daily patient reviewNaina Mohan, Gordon CaldwellGenetic Testing and Molecular Biomarkers|July 21, 2010
Chromosomal distribution of disease genes in the human genomeDavid N Cooper, Edward V Ball, Matthew MortHuman Mutation|May 6, 2008
A meta-analysis of nonsense mutations causing human genetic diseaseMatthew Mort, Dobril Ivanov, David N Cooper, et al.Obstetric Medicine|April 25, 2024
Streptococcus oralis meningitis in pregnancyNaina Mohan, Lucy O'Connor, Hannah Douglas, et al.Genome Research|July 14, 2011
Loss of exon identity is a common mechanism of human inherited diseaseTimothy Sterne-Weiler, Jonathan Howard, Matthew Mort, et al.Human Mutation|July 19, 2012
Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) geneLaura Thomas, Mark Richards, Matthew Mort, et al.Nucleic Acids Research|February 10, 2017
IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variantsCarolin Knecht, Matthew Mort, Olaf Junge, et al.European Journal of Human Genetics : EJHG|April 24, 2014
Identification of two novel SMCHD1 sequence variants in families with FSHD-like muscular dystrophyJincy Winston, Laura Duerden, Matthew Mort, et al.Pageof 9