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Vnitrni Lekarstvi
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October 1, 1993
[Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)]
K Indrák, V Divoký, V Brabec, et al.
Vnitrni Lekarstvi
|
November 20, 1998
[Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies]
K Indrák, V Divoký, E Kynclová, et al.
Rozhledy V Chirurgii : Mesicnik Ceskoslovenske Chirurgicke Spolecnosti
|
July 23, 2014
[Comparison between femoropopliteal bypass and subintimal recanalization in the treatment of critical limb ischaemia]
J Fialová, P Utíkal, M Köcher, et al.
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.
Vnitrni Lekarstvi
|
January 12, 2005
[New beta0-thalassaemic insertion mutation (CD 7/8, +G) in a Slovak family, associated with the Mediterranean haplotype IX]
E Kynclová, V Divoký, L Kovaríková, 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.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti
|
December 23, 2015
[Hepatoblastoma, Etiology, Case Reports]
A Puchmajerová, A Křepelová, J Indráková, et al.
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Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Vnitrni Lekarstvi
|
October 1, 1993
[Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)]
K Indrák, V Divoký, V Brabec, et al.
Vnitrni Lekarstvi
|
November 20, 1998
[Hemoglobin Sydney--alpha beta 2 67 (E11) Val-Ala and hemoglobin Olomouc alpha 2 beta 2 86 (F 2) Ala-Asp in Czech families. DNA sequence analysis for a more accurate diagnosis of hemoglobinopathies]
K Indrák, V Divoký, E Kynclová, et al.
Rozhledy V Chirurgii : Mesicnik Ceskoslovenske Chirurgicke Spolecnosti
|
July 23, 2014
[Comparison between femoropopliteal bypass and subintimal recanalization in the treatment of critical limb ischaemia]
J Fialová, P Utíkal, M Köcher, et al.
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.
Vnitrni Lekarstvi
|
January 12, 2005
[New beta0-thalassaemic insertion mutation (CD 7/8, +G) in a Slovak family, associated with the Mediterranean haplotype IX]
E Kynclová, V Divoký, L Kovaríková, 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.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti
|
December 23, 2015
[Hepatoblastoma, Etiology, Case Reports]
A Puchmajerová, A Křepelová, J Indráková, et al.
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