Hemoglobin Q-Thailand and its Combinations with other Forms of Thalassemia or Hemoglobinopathies in Northern Thailand
Author:
Publisher
Clinical Laboratory Publications
Subject
General Biochemistry, Genetics and Molecular Biology
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Two patients with α-chain hemoglobin variant Hb Q-Iran detected by measuring hemoglobin A1c using the variant mode of the HA-8180V HPLC analyzer;Diabetology International;2024-01-06
2. Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease;Hemoglobin;2018-01-02
3. Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family;Hemoglobin;2017-01-02
4. First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok;Hemoglobin;2016-11
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