Disorders of sex development as a part of developmental syndromes

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

Male pseudohermaphroditismevaluation in Egyptian Children

Sex chromosomal mosaicism in the gonads of patients with disorders of sex development

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

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

Analysis of kal-1 gene in Egyptian males with hypogonadotropic hypogonadism associated with anosmia

Genetic study of neural tube defects

Mullerian duct dysgenesis