Clinical Characterization of 53 Egyptian children diagnosed as Duchenne Muscular Dystrophy in tertiary unit in upper Egypt

Clinical and Molecular Characterization of Achondroplasia in Egyptian Patients

Molecular Study of the D1S80 Locus in Sample of Egyptian Population

Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder

DETECTION OF COMMON BETA THALASSEMIA MUTATIONS AMONG EGYPTIAN PATIENTS

Relation between Mir-196a2 and Mir-146a Polymorphisms and Susceptibility to DM1 in Egyptian Children

Clinical and Molecular Study of Exons [10-14] of ABCB11 Gene in PFIC2 Patients in Egypt

MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS

Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease

Clinical and Genetic Study of Exons (23, 24, 26, 27) of ABCB11 Gene in Egyptian Progressive Familial Intrahepatic Cholestasis 2 Patients