Association between XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patient

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

Prevalence of HbS Gene in Marzouk Region of Southern Libya

The prevalence of HBG2 polymorphism among Beta Thalassemia major Children in El Minia Governorate and its correlations with HbF level.

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

Hematological parameters in Myeloproliferative neoplasms in Sudanese patients

SNP in Tumor Necrosis Factor-Alpha (−308 A/G) Gene ‎ Association with HCV Infected Thalassemia Patients

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

The role of Interferon- γ Receptor-1 Gene (-56 T < C) polymorphism in development of susceptibility to pulmonary Tuberculosis in Central Sudan

Clinical and hematoloical complications in children with sickle-cell disease at Assuit University Children Hospital