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Hemoglobin|January 10, 2020
A Japanese Family with the Unstable Hb Sydney (HBB: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen SaturationAtsushi Sakamoto, Hisaya Nakadate, Kinji Tada, et al.
Hemoglobin|September 2, 2020
Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West IranKeivan Moradi, Mozaffar Aznab, Susan Tahmasebi, et al.
Hemoglobin|September 11, 2020
Hb A2-Pistoia [δ89(F5)Ser→Asn, HBD: c.269G>a]: a Novel Mutation on the δ-Globin Gene in an Italian ChildAdriana Guastini, Leonardo Rizzi, Fabiano Santoni, et al.
Hemoglobin|February 4, 2020
The Importance of Characterizing the Hemoglobin Instability of New Variants: The Case of Hb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C]Etienne Mondesert, Muriel Giansily Blaizot, Olivier Tournilhac, et al.
Hemoglobin|March 4, 2020
Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid ChromatographyRanjeet S Mashon, Reena Das, Radhika Dhawan, et al.
Hemoglobin|January 25, 2019
First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin GeneXiao-Hong He, Rui Zhang, Guang-Xing Mai, et al.
Hemoglobin|January 8, 2019
Hb Sichuan [α67(E16)Thr→Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin ElectrophoresisAn-Ping Xu, Wei-Dong Chen, Jie Li, et al.
Hemoglobin|December 19, 2017
A Novel α-Thalassemia Nonsense Mutation on the α2-Globin Gene: HBA2: c.184A>TYuan Liang, Qi Peng, Miao Li, et al.
Hemoglobin|December 19, 2017
Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, ThailandWansa Banyatsuppasin, Sumalee Jindadamrongwech, Anchalee Limrungsikul, et al.
Hemoglobin|November 30, 2018
A Rare Hb H Hydrops Fetalis Syndrome Caused by the - -SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese PatientQiang Li, Yihong Li, Mei Zhong, et al.
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