Genetic study in Egyptian children with Wilson disease

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

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

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

Molecular study and carrier detection of alpha thalassaemia in egypt

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

Metachromatic leukodystrophy in Egyptianchildren with dysmyelinating brain disease

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

The prevalence of p53 gene mutation in hepatocellular carcinoma in Egyptians