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

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

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

Identification of common mutationscausing Wilson disease in Egyptian children

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

G6PD gene polymorphisms in Egyptian deficient patients

Molecular study and carrier detection of alpha thalassaemia in egypt

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

Genetic polymorphism of microsomal epoxide hydrolase among a group of Egyptian acquired aplastic anemia patients

Genetic study in Egyptian children with Wilson disease