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   Chapter DOI:10.5005/jp/books/10900_20      

Beta-globin gene, Beta-thalassemia mutations, Carrier screening, Chronic liver disease, Classes of thalassemias, Diagnosis of thalassemia, Disorders of hemoglobin, Iron absorption, HbS mutation, Hemoglobin molecule, Hemoglobinopathies, Prenatal diagnosis, Sickle cell hemoglobinopathy, Splenectomy in thalassemia