Authors: Kemperman, MH Stinckens, C Kumar, S Huygen, PLM Joosten, FBM Cremers, CWRJ

Citation: Mh. Kemperman et al., Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome, OTOL NEURO, 22(5), 2001, pp. 637-643

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: Fransen, E Verstreken, M Bom, SJH Lemaire, F Kemperman, MH De Kok, YJM Wuyts, FL Verhagen, WIM Huygen, PLM McGuirt, WT Smith, RJH Van Maldergem, L Declau, F Cremers, CWRJ Van de Heyning, PH Cremers, FPM Van Camp, G

Citation: E. Fransen et al., A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation, J MED GENET, 38(1), 2001, pp. 61-64

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

Authors: Bom, SJH Kemperman, MH De Kok, YJM Huygen, PLM Verhagen, WIM Cremers, FPM Cremers, CWRJ

Citation: Sjh. Bom et al., Progressive cochleovestibular impairment caused by a point mutation in theCOCH gene at DFNA9, LARYNGOSCOP, 109(9), 1999, pp. 1525-1530