DETECTION OF COMMON BETA THALASSEMIA MUTATIONS AMONG EGYPTIAN PATIENTS

Characterization of the Molecular Spectrum of a-Thalassemia Mutations in the Western Province of Saudi Arabia and Recommendation for Premarital Screening

A Study of Hepcidin Gene Polymorphism in Beta Thalassemia Major Egyptian Patients Refractory to Iron Chelation

Glycometabolic Disorders in Patients with Β -Thalassemia Major in Egypt

Molecular and Hematological Analysis of Alpha Thalassemia in Middle East Patients; A Cross-Sectional Retrospective Study

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

Hemoglobin A2 Cut off Values in Egyptian Cohort as a marker of β -Thalassemia carriers.

Relation between nutritional status and inherited disorders of hemoglobin (thalassemia) in Egyptian children

Assessment of Molecular Changes of Transfusion Dependent Beta Thalassemia Children in El Minia Governorate and Their Correlations with Patients Clinical Outcomes

Hereditary Persistence of Fetal Hemoglobin and Genetic Heterogeneity in Alexandria, Egypt