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Journal of Medical Genetics|May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing lossL Morlé, M Bozon, N Alloisio, et al.
Hearing Research|October 27, 2004
Effect of stimulus frequency and stimulation site on the N1m response of the human auditory cortexD Gabriel, E Veuillet, R Ragot, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
Genetics and Molecular Research : GMR|November 26, 2016
Frequency of the Val1016Ile mutation on the kdr gene in Aedes aegypti (Diptera: Culicidae) in south BrazilM L Collet, C Frizzo, E Orlandin, et al.
Journal De Mycologie Medicale|December 28, 2020
Fungemia in the French department of Mayotte, Indian Ocean: A 10 years surveyR Wankap, C Mogo, M Niang, et al.
Journal of Clinical Microbiology|December 14, 2011
Human leptospira isolates circulating in Mayotte (Indian Ocean) have unique serological and molecular featuresP Bourhy, L Collet, T Lernout, et al.
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