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Fischel-Ghodsian, N (1999) Genetic factors in aminoglycoside toxicity. Ann N Y Acad Sci 884:99-109
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Casano, R A; Johnson, D F; Bykhovskaya, Y et al. (1999) Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications. Am J Otolaryngol 20:151-6
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Verhoeven, K; Ensink, R J; Tiranti, V et al. (1999) Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene. Eur J Hum Genet 7:45-51
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Fischel-Ghodsian, N (1999) Mitochondrial deafness mutations reviewed. Hum Mutat 13:261-70
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Fischel-Ghodsian, N (1998) Mitochondrial RNA processing and translation: link between mitochondrial mutations and hearing loss? Mol Genet Metab 65:97-104
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Fischel-Ghodsian, N (1998) Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics. Am J Hum Genet 62:15-9
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Johnson, D F; Hamon, M; Fischel-Ghodsian, N (1998) Characterization of the human mitochondrial ribosomal S12 gene. Genomics 52:363-8
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Fischel-Ghodsian, N (1998) Mitochondrial genetics and hearing loss: the missing link between genotype and phenotype. Proc Soc Exp Biol Med 218:1-6
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