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

DETECTION OF COMMON BETA THALASSEMIA MUTATIONS AMONG EGYPTIAN PATIENTS

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

MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS

Association between TBX20 gene polymorphism and congenital heart disease among Egyptian subjects

Molecular Diagnosis of Hepatocellular Carcinoma in Egypt

Genetic investigations on certain genes associated with type 1 diabetes in some Egyptions

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