Genotype and phenotype correlation in glucose-6- phosphate dehydrogenase deficiency

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

Molecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children

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

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

DNA repair gene xrcc1 polymorphism in Egyptian acute leukemia patients

Study of VKORC1 polymorphism (C1173T) in Egyptian population

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

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

Identification of common mutationscausing Wilson disease in Egyptian children