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Human Genetics|June 1, 2000
High frequency hearing loss correlated with mutations in the GJB2 geneS A Wilcox, K Saunders, A H Osborn, et al.Journal of Medical Genetics|January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing lossM J Houseman, L A Ellis, A Pagnamenta, et al.The Medical Journal of Australia|October 6, 2001
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafnessH H Dahl, K Saunders, T M Kelly, et al.ACS Materials Letters|January 10, 2025
3D-Printable Elastomers for Real-Time Autonomous Self-Healing in Soft DevicesJoseph G Beckett, Carl J Thrasher, Joshua Michonski, et al.Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.Pageof 6