Identification of common mutationscausing Wilson disease in Egyptian children

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

A study of the mitochondrial DNA mutations in diabetic patients

Molecular study and carrier detection of alpha thalassaemia in egypt

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

Metachromatic leukodystrophy in Egyptianchildren with dysmyelinating brain disease

A clinical and molecular genetic study on Egyptian children with hypertrophic cardiomyopathy

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

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

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