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Human Heredity|February 17, 1998
Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from SlovakiaM Plásilová, E Feráková, L Kádasi, et al.General Physiology and Biophysics|February 19, 2008
Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from SlovakiaI Zmetáková, V Ferák, G Minárik, et al.Bratislavske Lekarske Listy|February 1, 1992
[Rapid prenatal diagnosis of cystic fibrosis using the polymerase chain reaction: results of the first 5 cases]J Gécz, P Magdolen, V Tomová, et al.Human Genetics|May 1, 1992
Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patientsL Kádasi, J Gécz, J Matúsek, et al.Bratislavske Lekarske Listy|April 1, 1994
[DNA analysis in classic phenylketonuria--screening for mutations and haplotype analysis in Slovak families]L Kádasi, H Poláková, E Feráková, et al.Bratislavske Lekarske Listy|March 1, 1992
[The delta F508 mutation which causes cystic fibrosis and its association with closely linked DNA polymorphisms in the Slovak population]L Kádasi, J Gécz, A Puliti, et al.Human Genetics|January 1, 1995
PKU in Slovakia: mutation screening and haplotype analysisL Kádasi, H Poláková, E Feráková, et al.American Journal of Human Genetics|October 6, 2000
High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spotsA Zatková, D B de Bernabé, H Poláková, et al.Pageof 2