Study of the association between the -2518g/a polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene and myocardial infarction in the Egyptian patients

Clinical biochemical markers for hepatocellular carcinoma in Egyptian patients

The co-existance of β-fibrinogen -455 G/A polymorphism and prothrombin 20210 G/A mutation in coronary heart disease in Egyptan patients

Genetic Polymorphism of Uridine-Diphosphoglucuronosyl transferase 1A7 gene in chronic viral hepatitis and hepatocellular carcinoma in Egyptian patients

The study of polymorphism of the gene regulating region of the monocytechemoattractant protein-1 (MCP-1) insystemic lupus erythematosus

Study of the role of CYP17 gene polymorphismin polycystic ovary syndrome

TNF promoter -308 G>A and LTA 252 A>G polymorphisms in Egyptian patients with Systemic Lupus erythematosus

Thrombophilic gene mutations in cases with recurrent miscarriage : A study in the Egyptian Population

Vascular endothelial growth factor 634G/C gene polymorphism in prognosis of hepatocellular carcinoma in Egyptian patients

Genetic polymorphism of microsomal epoxide hydrolase among a group of Egyptian acquired aplastic anemia patients