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Results: 1-9 |
Results: 9
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus
Authors: Wayne, S Robertson, NG DeClau, F Chen, N Verhoeven, K Prasad, S Tranebjarg, L Morton, CC Ryan, AF Van Camp, G Smith, RJH
Citation: S. Wayne et al., Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus, HUM MOL GEN, 10(3), 2001, pp. 195-200
Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9
Authors: Robertson, NG Resendes, BL Lin, JS Lee, C Aster, JC Adams, JC Morton, CC
Citation: Ng. Robertson et al., Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9, HUM MOL GEN, 10(22), 2001, pp. 2493-2500
A novel conserved cochlear gene, OTOR: Identification, expression analysis, and chromosomal mapping
Authors: Robertson, NG Heller, S Lin, JS Resendes, BL Weremowicz, S Denis, CS Bell, AM Hudspeth, AJ Morton, CC
Citation: Ng. Robertson et al., A novel conserved cochlear gene, OTOR: Identification, expression analysis, and chromosomal mapping, GENOMICS, 66(3), 2000, pp. 242-248
Genomic structure of the human unconventional myosin VI gene
Authors: Ahituv, N Sobe, T Robertson, NG Morton, CC Taggart, RT Avraham, KB
Citation: N. Ahituv et al., Genomic structure of the human unconventional myosin VI gene, GENE, 261(2), 2000, pp. 269-275
High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene
Authors: Fransen, E Verstreken, M Verhagen, WIM Wuyts, FL Huygen, PLM D'Haese, P Robertson, NG Morton, CC McGuirt, WT Smith, RJH Declau, F Van de Heyning, PH Van Camp, G
Citation: E. Fransen et al., High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene, HUM MOL GEN, 8(8), 1999, pp. 1425-1429
Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness
Authors: Skvorak, AB Weng, ZP Yee, AJ Robertson, NG Morton, CC
Citation: Ab. Skvorak et al., Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness, HUM MOL GEN, 8(3), 1999, pp. 439-452
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
Authors: de Kok, YJM Bom, SJH Brunt, TM Kemperman, MH van Beusekom, E van der Velde-Visser, SD Robertson, NG Morton, CC Huygen, PLM Verhagen, WIM Brunner, HG Cremers, CWRJ Cremers, FPM
Citation: Yjm. De Kok et al., A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects, HUM MOL GEN, 8(2), 1999, pp. 361-366
Leo Strauss and the American right.
Authors: Robertson, NG
Citation: Ng. Robertson, Leo Strauss and the American right., J POLIT, 61(1), 1999, pp. 261-263
Beginning of a molecular era in hearing and deafness
Authors: Robertson, NG Morton, CC
Citation: Ng. Robertson et Cc. Morton, Beginning of a molecular era in hearing and deafness, CLIN GENET, 55(3), 1999, pp. 149-159
Risultati: 1-9 |