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

DETECTION OF COMMON BETA THALASSEMIA MUTATIONS AMONG EGYPTIAN PATIENTS

MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS

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

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

Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening

A Review of β-Thalassemia in Saudi Arabian Children

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

Role of Alpha Hemoglobin Stabilizing Protein Expression in Beta Thalassemia Patients

Pattern and clinical profile of thalassemia among pediatric patients attending the Yemeni Society Centers for Thalassemia and Genetic Blood Disorders in Yemen