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Hemoglobin
international journal for hemoglobin research
Volume 41, 2017 - Issue 3
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Short Communication

Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia

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Pages 203-208 | Received 26 Nov 2016, Accepted 14 May 2017, Published online: 03 Jul 2017

Keep up to date with the latest research on this topic with citation updates for this article.

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Qiong Su, Shiping Chen, Liusong Wu, Runmei Tian, Xiaoqin Yang, Xiaoyan Huang, Yan Chen, Zhiyu Peng & Jindong Chen. (2019) Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene. Hemoglobin 43:1, pages 7-11.
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Articles from other publishers (2)

Qin Zhang, Yujia Huo, Qinggang Sun, Nan Liu, Hongchuan Shi, Minghui Wang, Jinming Xiao, Hanzi Yuan & Xiangfeng Tang. (2023) Case report: Curing a rare, unstable hemoglobin variant Hb Bristol-Alesha using haploidentical hematopoietic stem cell transplantation. Frontiers in Immunology 14.
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Shanshan Li, Kai Chen, Can Huang, Na Zhang, Hui Jiang & Shayi Jiang. (2021) First report of successful treatment for hemoglobin Bristol-Alesha by hemopoietic stem cell transplantation. Annals of Hematology 101:3, pages 617-619.
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