Authors: Kovach, MJ Ruiz, J Kimonis, K Mueed, S Sinha, S Higgins, C Elble, S Elble, R Kimonis, VE

Citation: Mj. Kovach et al., Genetic heterogeneity in autosomal dominant essential tremor, GENET MED, 3(3), 2001, pp. 197-199

Authors: Jonas, RE Kimonis, VE

Citation: Re. Jonas et Ve. Kimonis, Chest wall hamartoma with Wiedemann-Beckwith syndrome: Clinical report andbrief review of chromosome 11p15.5-related tumors, AM J MED G, 101(3), 2001, pp. 221-225

Authors: Kimonis, VE Kovach, MJ Waggoner, B Leal, S Salam, A Rimer, L Davis, K Khardori, R Gelber, D

Citation: Ve. Kimonis et al., Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone, GENET MED, 2(4), 2000, pp. 232-241

Authors: Kovach, MJ Lin, JP Boyadjiev, S Campbell, K Mazzeo, L Herman, K Rimer, LA Frank, W Llewellyn, B Jabs, EW Gelber, D Kimonis, VE

Citation: Mj. Kovach et al., A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness, AM J HU GEN, 64(6), 1999, pp. 1580-1593