The amount of Hb CS in those carrying Hb CS was 0.2–6.5% which showed an increasing trend according to the number of defective α-globin genes, in contrast to Hb A 2 levels, which decreased.
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Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis.
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