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Results: 1-6 |
Results: 6

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: Forrester, S Kovach, MJ Reynolds, NM Urban, R Kimonis, V
Citation: S. Forrester et al., Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome, AM J MED G, 98(1), 2001, pp. 92-100

Authors: Chen, AS Kovach, MJ Herman, K Avakian, A Frank, W Forrester, S Lin, JP Kimonis, V
Citation: As. Chen et al., Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families, GENET MED, 2(5), 2000, pp. 283-289

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: Haworth, PD Kovach, MJ Sperline, RP Raghavan, S
Citation: Pd. Haworth et al., Interaction of a polyglycidol-based nonionic surfactant with silicon in hydrofluoric acid solutions, J ELCHEM SO, 146(6), 1999, pp. 2284-2288

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
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