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- W2009152471 abstract "Routine laboratory investigations of hemoglobinopathies include Hb electrophoresis for abnormal hemoglobins, determination of Hb A2 (alpha 2 delta 2) for beta-thalassemia traits, staining for Hb H (beta 4) inclusions for alpha-thalassemia traits and estimation of Hb F (alpha 2 lambda 2) for the presence of hereditary persistence of fetal hemoglobin genes (HPFH). Frequently, analytical column chromatography and alpha/beta hemoglobin chain synthesis are used in the studies of more complicated hemoglobinopathies. This communication outlines the procedures used in this laboratory for the diagnosis of a case of Hb CC-alpha-thalassemia." @default.
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- W2009152471 modified "2023-09-27" @default.
- W2009152471 title "Laboratory diagnosis of HB CC-α-thalassemia" @default.
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- W2009152471 doi "https://doi.org/10.1016/s0009-9120(79)80080-6" @default.
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