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British Journal of Haematology|December 6, 2017
Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in CameroonAmbroise Wonkam, Khuthala Mnika, Valentina J Ngo Bitoungui, et al.
Experimental Biology and Medicine (Maywood, N.J.)|September 30, 2020
Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairmentOluwafemi G Oluwole, Kevin K Esoh, Edmond Wonkam-Tingang, et al.
Genes|November 27, 2025
Whole-Exome Sequencing for Molecular Diagnosis of Paediatric Nephrotic Syndrome in Africa: A Call for ImplementationThina Gcobo, Jonathan N Katsukunya, Lindie Lamola, et al.
Bioinformatics (Oxford, England)|September 29, 2017
A multi-scenario genome-wide medical population genetics simulation frameworkJacquiline W Mugo, Ephifania Geza, Joel Defo, et al.
Genes|February 27, 2020
Hearing Impairment Overview in Africa: the Case of CameroonEdmond Wonkam Tingang, Jean Jacques Noubiap, Jean Valentin F Fokouo, et al.
Frontiers in Molecular Biosciences|July 23, 2024
Network-based integrative multi-omics approach reveals biosignatures specific to COVID-19 disease phasesFrancis E Agamah, Thomas H A Ederveen, Michelle Skelton, et al.
British Journal of Haematology|May 4, 2017
Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in CameroonAmy Geard, Gift D Pule, Bernard Chetcha Chemegni, et al.
Briefings in Bioinformatics|May 19, 2017
Large-scale data-driven integrative framework for extracting essential targets and processes from disease-associated gene data setsGaston K Mazandu, Emile R Chimusa, Kayleigh Rutherford, et al.
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