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The American Journal of Otology|January 26, 1999
Cracking the auditory genetic code: nonsyndromic hereditary hearing impairmentA K Lalwani, C M CasteleinAmerican Journal of Human Genetics|October 12, 2000
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9A K Lalwani, J A Goldstein, M J Kelley, et al.Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.Pageof 1