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Vnitrni Lekarstvi|June 8, 1999
[Haplotypes of the beta-globulin locus in Czechs and Slovaks with beta-thalassemia and structurally variant hemoglobins]E Kynclová, L Kovaríková, P Fajkosová, et al.
Annals of Hematology|August 1, 1994
Hb Nottingham or alpha 2 beta 2 98 (FG5) Val-->Gly in a Czech childV Brabec, K Indrák, H Fortová, et al.
Annals of Hematology|July 1, 1991
A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplicationK Indrak, Y J Fei, H W Li, et al.
Vnitrni Lekarstvi|April 1, 1994
[Dominant beta-thalassemia alleles in the Czech and Slovak population (beta-thalassemia mutations in 112(T-A) and 121(G-T) codons and the unstable Hradec Králové hemoglobin or alpha 2 beta 2 115 (G17) Ala-Asp)]K Indrák, V Divoký, V Brabec, et al.
Blood|February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
Dalton Transactions (Cambridge, England : 2003)|April 28, 2023
Triplex metallohelices have enantiomer-dependent mechanisms of action in colon cancer cellsJ P C Coverdale, H Kostrhunova, L Markova, et al.
Human Genetics|February 1, 1992
Molecular characterization of beta-thalassemia in CzechoslovakiaK Indrak, V Brabec, J Indrakova, et al.
Blood|July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiencyH Hassoun, J N Vassiliadis, J Murray, et al.
The Journal of Clinical Investigation|January 1, 1994
Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)P Jarolim, H L Rubin, S C Liu, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
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