Study of methylenetetraydrofolate reductase gene mutation as a risk factor for deep venous thrombosis

Assessment of factor V leiden, prothrombin gene mutation and methylenetetrahydrofolate reductase activity in pediatric patients with thalassemia

Association of Factor XII genotypic polymorphism and phenotype with risk of venous thrombosis

Study of factor V liden in thromboembolic patients

The clinical impact of methylene tetrahydrofolate reductase polymorphism on the vascular complications of sickle cell disease

Prevelance of activated protein c resistance among patients with venous thromboembolism

Impact of prothrombotic risk factors on the clinical phenotype in haemophilia patients

The role of plasma homocysteine and its genetic control as risk factors for thrombophilia

Influence of Iron Regulating genes mutations on iron overload in sickle cell disease

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