Association of the protein Z intron F G79A and IL-6 C634 G genes polymorphisms with recurrent pregnancy loss in Egyptian females

Thrombophilic Gene Mutation and Correlation to Recurrent Miscarriage: An Egyptian Study

Study of VKORC1 polymorphism (C1173T) in Egyptian population

Molecular study of factor VIII gene in Egyptian patients with hemophilia A

A pilot study for the prevalence of methylenetetrahydrofolate reductase gene mutation in Egyptian children with homocystinuria

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

DNMT3B 579G>T promoter polymorphism and the risk for idiopathic thrombocytopenic purpura : An Egyptian study

Identification of some genetic markers in familial breast cancer in Egyptian patients

Mutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia

Endothelial nitric oxide synthase gene polymorphism in women with spontaneous recurrent miscarriage