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