الفهرس 
Thalassemia Syndromes
Assessment of renal functionsOnly 14 pages are availabe for public view
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Abstract
Beta thalassemia syndromes are a group of hereditary disorders characterized by genetic deficiency in the synthesis of beta globin chains in B-thalassemia major the production of beta-globin chains is severely impaired because both beta-globin genes are mutated on chromosome II.