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Hemoglobin|September 7, 2000
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levelsR Oner, E Birben, C Acar, et al.Hemoglobin|September 7, 2000
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levelsC Vrettou, E Kanavakis, J Traeger-Synodinos, et al.Hemoglobin|September 7, 2000
Sickle cell anemia and beta-globin gene cluster haplotypes in ColombiaF Cuéllar-Ambrosi, M C Mondragón, M Figueroa, et al.Hemoglobin|May 21, 1999
Capillary zone electrophoresis: an additional technique for the identification of hemoglobin variantsC Lin, F Cotton, B Fontaine, et al.Hemoglobin|September 18, 1999
The precise breakpoints of a Filipino-type alpha-thalassemia-1 deletion found in two JapaneseY Hattori, N Okayama, Y Ohba, et al.Hemoglobin|April 13, 2001
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patientsC Bincoletto, R C Perlingeiro, S T Saad, et al.Hemoglobin|April 13, 2001
Hb Sitia [beta128(H6)Ala-->Val]: an unstable variant with a substitution in the alpha1beta1 interfaceI Papassotiriou, J Traeger-Synodinos, D Promé, et al.Hemoglobin|April 13, 2001
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemiaP Rigano, G P Rodgers, D Renda, et al.Hemoglobin|March 19, 1999
Southeast Asian ovalocytosis in White personsP O Schischmanoff, T Cynober, F Miélot, et al.Hemoglobin|September 26, 2001
Could capillary zone electrophoresis of tryptic peptides be used for the characterization of hemoglobin variants?C Lin, B Gulbis, E Delobbe, et al.Pageof 240