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

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

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

Identification of common mutationscausing Wilson disease in Egyptian children

Congenital adrenal hyperplasia due to11 β hydroxylase deficiency : A clinical and diagnostic approach

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

Thyroid peroxidese gene mutation in congenitalhypothyroidism

Genetic study in Egyptian children with Wilson disease

Male pseudohermaphroditismevaluation in Egyptian Children

G6PD gene polymorphisms in Egyptian deficient patients