Identification of common mutationscausing Wilson disease in Egyptian children

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

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

Some potential genetic markers for prediction of treatment response in HCV affected Egyptian children

Molecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies

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

Metachromatic leukodystrophy in Egyptianchildren with dysmyelinating brain disease

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

Ultrastructrural analysis of hepatic tissue copper and iron in Egyptian children with chronic liver diseases

Molecular study and carrier detection of alpha thalassaemia in egypt