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:
Herman, K
Gruchala, A
Niezabitowski, A
Glinski, B
Lackowska, B
Citation: K. Herman et al., Prognostic factors in retroperitoneal sarcomas: Ploidy of DNA as a predictor of clinical outcome, J SURG ONC, 71(1), 1999, pp. 32-35
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