Detection of factor V leidenmutation in children with portal vein thrombosis

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

Genetic variation in coagulation factors and their impact on arterial and venous thrombosis

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

Study of factor V liden in thromboembolic patients

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

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

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

Methylenetetrahydrofolate reductase gene mutation as a predisposing factor for primary deep venous thrombosis