Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease
Author:
Affiliation:
1. Department of Medical Technology, Faculty of Allied Health Sciences, Phayao University, Phayao, Thailand;
2. Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand
Funder
University of Phayao
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1430587
Reference14 articles.
1. Three cases of Hb Q-H disease found in a Cantonese family
2. Hb Q-Thailand [α74(EF3)Asp→His]: Gene Organization, Molecular Structure, and DNA Diagnosis
3. Detection of Compound Heterozygous of Hb Constant Spring and Hb Q-Thailand by Capillary Electrophoresis and High Performance Liquid Chromatography
4. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy
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1. Asymptomatic Co-Inheritance of Hb Leiden (HBB:c.22_24delGAG), Hb Q-Thailand (HBA1:c.223G > C) and Deletional Alpha Thalassemia in a Young Chinese Male;Indian Journal of Hematology and Blood Transfusion;2024-05-16
2. Molecular Characterization of α‐ and β‐Thalassemia Among Children Less Than 18 Years Old in Guizhou, China;Journal of Clinical Laboratory Analysis;2024-03
3. When Hemoglobin Reported to Be A, S, and F Are Neither A, S, Nor F: A Tale of Two Patients;The Journal of Applied Laboratory Medicine;2020-09-30
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