Two families from southern India with members having the clinical manifestations of thalassemia intermedia are presented. Hematologic and globin chain synthesis data indicated that in one family the affected brother and sister had the β+- δ° β°-thalassemia condition while in the other family the propositus was homozygous for a β°-thalassemia determinant.
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© 1980 S. Karger AG, Basel
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