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

Epidemiology and clinical characters of congenital adrenal hyperplasia patientsattending endocrinology Clinic at CairoUniversity Children’s Hospital

Clinical phenotypes of renal cystic diseases in Egyptian children

Mucopolysaccharidosis in Egyptian children : Clinical and biochemical profile of 20 cases

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

A clinical study of aplastic anemia : Ten years experience of a single Egyptian pediatric hematology unit

Study of 1, 25 dihydroxycholecalciferol and its relation to bone mineral density and heart disease in Egyptian beta thalessmia patients

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

Clinical and Molecular Characterization of Achondroplasia in Egyptian Patients

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