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Hemoglobin|May 20, 2020
A New α Chain Variant, Hb Heilongjiang (<i>HBA2</i>: c.49A>C), Found During Hb A<sub>1c</sub> MeasurementAnping Xu, Weidong Chen, Weijie Xie, et al.
Hemoglobin|June 19, 2015
Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia IntermediaSamaneh Farashi, Nooshin Bayat, Negin Faramarzi Garous, et al.
Hemoglobin|June 24, 2015
Description of Three New α Variants and Four New β Variants: Hb Montluel [α110(G17)Ala → Val; HBA1: c.332C > T], Hb Cap d'Agde [α131(H14)Ser → Cys; HBA2: c.395C > G] and Hb Corsica [α100(G7)Leu → Pro; HBA1: 302T > C]; Hb Nîmes [β104(G6)Arg → Gly; HBB: c.313A > G], Hb Saint Marcellin [β112(G14)Cys → Gly; HBB: c.337T > G], Hb Saint Chamond [β80(EF4)Asn → 0; HBB: c.241_243delAAC] and Hb Dompierre [β29(B11)Gly → Arg; HBB: c.88G > C]Céline Renoux, Cécile Feray, Philippe Joly, et al.
Hemoglobin|June 16, 2015
Clinical and Molecular Characteristics of Non-Transfusion-Dependent Thalassemia in KuwaitAdekunle D Adekile, Asma F Azab, Sondus I Al-Sharida, et al.
Hemoglobin|June 27, 2015
Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and CanadaHira S Mian, Richard Ward, Paul Telfer, et al.
Hemoglobin|May 29, 2015
Molecular Diagnosis of α⁰-Thalassemia Through Urine DNA: A Novel DNA Source to Facilitate Prevention Programs in Remote Geographical AreasNarutchala Suwannakhon, Teerapat Seeratanachot, Khwanruedee Mahingsa, et al.
Hemoglobin|May 29, 2015
Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia PatientsAlice Pecoraro, Antonio Troia, Roberta Calzolari, et al.
Hemoglobin|May 29, 2015
Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia TraitMan-Yu Wu, Jian Li, Shu-Chen Li, et al.
Hemoglobin|May 29, 2015
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian PopulationIlhem Ben Charfeddine, Taheni Ben Lazreg, Ahlem M'sakni, et al.
Hemoglobin|June 6, 2015
Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian PopulationFatimetou Veten, Sidi Ghaber, Nordine Habti, et al.
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