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