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Results: 1-4 |
Results: 4

Authors: Campbell, C Cucci, RA Prasad, S Green, GE Edeal, JB Galer, CE Karniski, LP Sheffield, VC Smith, RJH
Citation: C. Campbell et al., Pendred syndrome, DFNB4, and PDS/SCL26A4 identification of eight novel mutations and possible genotype-phenotype correlations, HUM MUTAT, 17(5), 2001, pp. 403-411

Authors: Van Laer, L Coucke, P Mueller, RF Caethoven, G Flothmann, K Prasad, SD Chamberlin, GP Houseman, M Taylor, GR Van de Heyning, CM Fransen, E Rowland, J Cucci, RA Smith, RJH Van Camp, G
Citation: L. Van Laer et al., A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment, J MED GENET, 38(8), 2001, pp. 515-518

Authors: Cucci, RA Prasad, S Kelley, PM Green, GE Storm, K Willocx, S Cohn, ES Van Camp, G Smith, RJH
Citation: Ra. Cucci et al., The M34T allele variant of Connexin 26, GENET TEST, 4(4), 2000, pp. 335-344

Authors: Prasad, S Cucci, RA Green, GE Smith, RJH
Citation: S. Prasad et al., Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA), HUM MUTAT, 16(6), 2000, pp. 502-508
Risultati: 1-4 |