HbE/β-Thalassemia: Basis of Marked Clinical Diversity
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology
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1. Clinical characteristics, laboratory features and genetic profile of hemoglobin E (HBB:c.79 G > A)/β (nucleotide -28 A > G) (HBB:c.-78 A > G) -thalassemia subjects identified from community- and hospital-recruited cohorts;Blood Cells, Molecules, and Diseases;2024-11
2. α-Globin mutations and Genetic Variants in γ-globin Promoters are Associated with Unelevated Hemoglobin F Expression of Atypical β0-thalassemia/HbE;Archives of Medical Research;2024-09
3. The Key Genetic Determinants Behind the Phenotypic Heterogeneity of HbE/β-thalassemia Patients and the Probable Management Strategy;Thalassemia Syndromes - New Insights and Transfusion Modalities;2023-11-22
4. Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/β-thalassemia prenatal genetic counseling;Blood Cells, Molecules, and Diseases;2023-11
5. Molecular understanding of unusual HbE-β + -thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels;Annals of Medicine;2023-10-10
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