The impact of iron regulating genes mutations on iron overload in β-thalassemia patients

Effect of HFE gene (hemochromatosis in iron) mutation on iron overload in thalassemic patients

Haemochromatosis gene mutations in chronic hepatitis C patients

Mannose binding lectin (MBL2) gene variants in sickle cell disease

Study of glutathione S-transferase gene polymorphisms in sickle cell anemia patients

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

Association of factor V leiden and prothrombin gene mutations with thrombotic risk in patients with sickle cell anemia

IL28B gene polymorphism and spontaneous hepatitis C virus clearance in sickle cell disease patients

DNA sequencing of uncharacterized β–globin gene mutations in β–thalassaemia in children