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: Bom, SJH De Leenheer, EMR Lemaire, FX Kemperman, MH Verhagen, WIM Marres, HAM Kunst, HPM Ensink, RJH Bosman, AJ Van Camp, G Cremers, FPM Huygen, PLM Cremers, CWRJ

Citation: Sjh. Bom et al., Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH, ARCH OTOLAR, 127(9), 2001, pp. 1045-1048

Authors: De Leenheer, EMR Kunst, HPM McGuirt, WT Prasad, SD Brown, MR Huygen, PLM Smith, RJH Cremers, WRJ

Citation: Emr. De Leenheer et al., Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13), ARCH OTOLAR, 127(1), 2001, pp. 13-17

Authors: McGuirt, WT Prasad, SD Griffith, AJ Kunst, HPM Green, GE Shpargel, KB Runge, C Huybrechts, C Mueller, RF Lynch, E King, MC Brunner, HG Cremers, CWRJ Takanosu, M Li, SW Arita, M Mayne, R Prockop, DJ Van Camp, G Smith, RJH

Citation: Wt. Mcguirt et al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13), NAT GENET, 23(4), 1999, pp. 413-419

Authors: Bom, SJH Kunst, HPM Huygen, PLM Cremers, FPM Cremers, CWRJ

Citation: Sjh. Bom et al., Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes, BR J AUDIOL, 33(5), 1999, pp. 335-348