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: Bespalova, IN Burmeister, M

Citation: In. Bespalova et M. Burmeister, Identification of a novel LIM domain gene, LMCD1, and chromosomal localization in human and mouse, GENOMICS, 63(1), 2000, pp. 69-74

Authors: Smith, B Shatz, R Elisevich, K Bespalova, IN Burmeister, M

Citation: B. Smith et al., Effects of vagus nerve stimulation on progressive myoclonus epilepsy of Unverricht-Lundborg type, EPILEPSIA, 41(8), 2000, pp. 1046-1048

Authors: Bespalova, IN Burmeister, M Lesperance, MM

Citation: In. Bespalova et al., No association between DFNA6 and Pro250Arg mutation in FGFR3, AM J MED G, 88(5), 1999, pp. 451-451

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