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Citation: T. Dork et al., Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe, HUM GENET, 106(3), 2000, pp. 259-268

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: Zat'kova, A Hahnen, E Wirth, B Kadasi, L

Citation: A. Zat'Kova et al., Analysis of the SMN and NAIP genes in Slovak spinal muscular atrophy patients, HUMAN HERED, 50(3), 2000, pp. 171-174

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