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Hemoglobin|March 10, 2018
Psychological Factors Associated with Episodic Chelation Adherence in ThalassemiaJane Vosper, Michael Evangeli, John B Porter, et al.Hemoglobin|August 26, 2017
α<sup>0</sup>-Thalassemia Due to a 90.7 kb Deletion (- -<sup>NFLD</sup>)John S Waye, Barry Eng, Meredith Hanna, et al.Hemoglobin|December 19, 2017
First Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese FamilyFan Jiang, Gui-Lan Chen, Jian-Ying Zhou, et al.Hemoglobin|May 16, 2022
A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β<sup>0</sup> Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (<i>HBB</i>: c.151A>T) mutation <i>in cis</i>]Juan Liao, Qin Li, Li-Qin Ling, et al.Hemoglobin|May 16, 2022
Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained SettingAnkita Sen, Aditi Sen, Tuphan Kanti DolaiHemoglobin|May 13, 2022
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia MajorLi Zhang, Li-Juan Bao, Zheng-Dong Hong, et al.Hemoglobin|January 1, 1987
Distribution of hemoglobin E and beta-thalassemia in Kampuchea (Cambodia)T Sanguansermsri, G Flatz, S D FlatzHemoglobin|July 26, 2021
The Effect of <i>HBB</i>: c.-121C>T Variant [-71 (C>T)] on the β-Globin Promoter: Case Series StudyMilad Rafat, Zeinab Allamehzadeh, Mohammad Shekari, et al.Hemoglobin|May 11, 2022
Dynamic Thiol-Disulfide Homeostasis in Children With β-Thalassemia TraitBurçak Kurucu, Ali Fettah, Emre Çapkınoğlu, et al.Hemoglobin|June 4, 2021
A Novel Mutation at <i>HBA1</i>: c.349G>T Causing α-Thalassemia in a Chinese FamilyZhenzhen Yin, Yuqi Hao, Xiaoyan Huang, et al.Pageof 238