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Brain Research. Brain Research Reviews|April 7, 2000
Connexin 26: required for normal auditory functionP M Kelley, E Cohn, W J KimberlingAmerican Journal of Medical Genetics|December 18, 2001
Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutationS Abe, P M Kelley, W J Kimberling, et al.Journal of Medical Genetics|January 14, 2000
Prevalent connexin 26 gene (GJB2) mutations in JapaneseS Abe, S Usami, H Shinkawa, et al.American Journal of Medical Genetics|March 2, 1999
Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred geneS Abe, S Usami, D M Hoover, et al.Genomics|December 28, 1999
Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12P M Kelley, S Abe, J W Askew, et al.American Journal of Human Genetics|June 13, 1998
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing lossP M Kelley, D J Harris, B C Comer, et al.Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.Human Mutation|September 30, 1999
Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.Journal of the American Academy of Audiology|January 1, 1995
Clinical and molecular genetics of Usher syndromeW J Kimberling, C MöllerPageof 88