Associated Papers
A Pragmatic Scoring Tool to Predict Hydroxyurea Response Among β-Thalassemia Major Patients in Pakistan.
Ansari SH et al.
Journal of Pediatric Hematology/oncology, 2022
Genetic epidemiology of hemoglobinopathies among Iraqi Kurds.
Al-Allawi N et al.
Journal of Community Genetics, 2021
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka.
Perera S et al.
Scientific Reports, 2019
Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine.
Faraon R et al.
Bmc Hematology, 2019
Annotated definition of BCL11A and HMIP-2 haplotypes through the analysis of sicilian β-thalassemia patients with high levels of fetal hemoglobin.
Buccheri MA et al.
Hemoglobin, 2013
Utility of the multivariate approach in predicting β-thalassemia intermedia or β-thalassemia major types In Iranian patients.
Banan M et al.
Hemoglobin, 2013
The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patients.
Banan M et al.
Hemoglobin, 2012
Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.
Al-Sultan A et al.
Hemoglobin, 2011
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