Authors: Bespalova, IN Van Camp, G Bom, SJH Brown, DJ Cryns, K DeWan, AT Erson, AE Flothmann, K Kunst, HPM Kurnool, P Sivakumaran, TA Cremers, CWRJ Leal, SM Burmeister, M Lesperance, MM

Citation: In. Bespalova et al., Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss, HUM MOL GEN, 10(22), 2001, pp. 2501-2508

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: Storm, K Willocx, S Flothmann, K Van Camp, G

Citation: K. Storm et al., Determination of the carrier frequency of the common GJB2 (Connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method, HUM MUTAT, 14(3), 1999, pp. 263-266

Authors: Van Camp, G Kunst, H Flothmann, K McGuirt, W Wauters, J Marres, H Verstreken, M Bespalova, IN Burmeister, M Van de Heyning, PH Smith, RJH Willems, PJ Cremers, CWRJ Lesperance, MM

Citation: G. Van Camp et al., A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus, J MED GENET, 36(7), 1999, pp. 532-536