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

DETECTION OF COMMON BETA THALASSEMIA MUTATIONS AMONG EGYPTIAN PATIENTS

Prenatal counseling and diagnosis of Gaucher disease in Egypt: an 18-year experience

MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS

Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants

A rare mutation in an Egyptian family with Sanfilippo B syndrome

Mutational Screening of (CLN6), (CLN7) and (CLN14) Genes in Egyptian Patients with Neuronal Ceroid Lipofuscinosis.

Prevalence of TP53 Gene Mutation in GBM Patients in Egyptian Population

Glycometabolic Disorders in Patients with Β -Thalassemia Major in Egypt

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