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Results: 1-5 |
Results: 5

Authors: Goth, L Shemirani, A Kalmar, T
Citation: L. Goth et al., A novel catalase mutation (a GA insertion) causes the Hungarian type of acatalasemia, BL CELL M D, 26(2), 2000, pp. 151-154

Authors: Goth, L Gorzsas, A Kalmar, T
Citation: L. Goth et al., A simple PCR-heteroduplex screening method for detection of a common mutation of the catalase gene in Hungary, CLIN CHEM, 46(8), 2000, pp. 1199-1200

Authors: Jakab, K Gardian, G Endreffy, E Kalmar, T Bachrati, C Vecsei, L Rasko, I
Citation: K. Jakab et al., Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in aHungarian population, EUR NEUROL, 41(2), 1999, pp. 107-110

Authors: Ivanyi, B Haszon, I Endreffy, E Szenohradszky, P Petri, IB Kalmar, T Butkowski, RJ Charonis, AS Turi, S
Citation: B. Ivanyi et al., Childhood membranous nephropathy, circulating antibodies to the 58-kD TIN antigen, and anti-tubular basement membrane nephritis: An 11-year follow-up, AM J KIDNEY, 32(6), 1998, pp. 1068-1074

Authors: Bachrati, CZ Somodi, Z Endreffy, E Kalmar, T Rasko, I
Citation: Cz. Bachrati et al., Carrier detection by microsatellite analysis of Duchenne Becker muscular dystrophy in Hungarian families, ANN HUM GEN, 62, 1998, pp. 511-520
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