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Hemoglobin|October 31, 2002
Hb G-Makassar [beta6(A3)Glu-->Ala; codon 6 (GAG-->GCG)]: molecular characterization, clinical, and hematological effectsVip Viprakasit, Aranya Wiriyasateinkul, Benjamas Sattayasevana, et al.
Hemoglobin|October 31, 2002
Molecular characterization of Hb D-Punjab [beta121(GH4)Glu-->Gln] in ThailandSupan Fucharoen, Yossombat Changtrakun, Sutja Surapot, et al.
Hemoglobin|October 31, 2002
Decreased morbidity in homozygous sickle cell disease detected at birthJosiane Bardakdjian-Michau, Monique Guilloud-Batailie, Micheline Maier-Redelsperger, et al.
Hemoglobin|February 27, 2003
The codons 8/9 (+G) mutation found for the first time in the Lebanese populationPierre A Zalloua, Elie Aoun, Suzanne Koussa, et al.
Hemoglobin|July 30, 2002
Compound heterozygosity for alpha0-thalassemia (- -THAI) and Hb constant spring causes severe Hb H diseaseVip Viprakasit, Voravarn S Tanphaichitr
Hemoglobin|January 17, 2002
Priapism in sickle cell anemia in Togo: prevalence and knowledge of this complicationA D Gbadoé, A Dogba, A Y Ségbéna, et al.
Hemoglobin|November 14, 2019
Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case reportAhmad Shoujaa, Yasser Mukhalalaty, Hossam Murad, et al.
Hemoglobin|November 6, 2019
Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary ElectrophoresisKunyakan Khongthai, Chedtapak Ruengdit, Sitthichai Panyasai, et al.
Hemoglobin|November 7, 2019
Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C)Ya-Li Lei, Hong Sui, Yu-Juan Liu, et al.
Hemoglobin|February 1, 2019
An Additional Case of Hb Saint Nazaire [β103(G5)Phe→Ile; HBB: c.310T>A] Leading to Moderate Erythrocytosis in a French FamilyVictor Bobée, Guillaume Feugray, Valéry Brunel, et al.
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