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
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