Authors:
Zatkova, A
Polakova, H
Micutkova, L
Zvarik, M
Bosak, V
Ferakova, E
Matusek, J
Ferak, V
Kadasi, L
Citation: A. Zatkova et al., Novel mutations in the homogentisate-1,2-dioxygenase gene identified in Slovak patients with alkaptonuria, J MED GENET, 37(7), 2000, pp. 539-542
Authors:
Zatkova, A
de Bernabe, DBV
Polakova, H
Zvarik, M
Ferakova, E
Bosak, V
Ferak, V
Kadasi, L
de Cordoba, SR
Citation: A. Zatkova et al., High frequency of alkaptonuria in Slovakia: Evidence for the appearance ofmultiple mutations in HGO involving different mutational hot spots, AM J HU GEN, 67(5), 2000, pp. 1333-1339
Authors:
Kivisild, T
Bamshad, MJ
Kaldma, K
Metspalu, M
Metspalu, E
Reidla, M
Laos, S
Parik, J
Watkins, WS
Dixon, ME
Papiha, SS
Mastana, SS
Mir, MR
Ferak, V
Villems, R
Citation: T. Kivisild et al., Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages, CURR BIOL, 9(22), 1999, pp. 1331-1334
Authors:
Plasilova, M
Stoilov, I
Sarfarazi, M
Kadasi, L
Ferakova, E
Ferak, V
Citation: M. Plasilova et al., Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma, J MED GENET, 36(4), 1999, pp. 290-294