Compound Heterozygous Hb Tak/Hb E Causes Secondary Erythrocytosis in a Thai Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630261003680498
Reference13 articles.
1. Hemoglobins with High Oxygen Affinity Leading to Erythrocytosis. New Variants and New Concepts
2. HÆMOGLOBIN TAK: A VARIANT WITH ADDITIONAL RESIDUES AT THE END OF THE β-CHAINS
3. Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group
4. Homozygous Hemoglobin Tak Causes Symptomatic Secondary Polycythemia in a Thai Boy
Cited by 6 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. Recurrent Intracranial Hemorrhages in a Patient With Hb Tak and Hb E;Annals of Internal Medicine: Clinical Cases;2024-06-01
2. Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis;Indian Journal of Hematology and Blood Transfusion;2017-04-04
3. Secondary erythrocytosis caused by hemoglobin Tak/β0-thalassaemia disease during pregnancy: A case report;Journal of Obstetrics and Gynaecology;2016-12-14
4. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system;International Journal of Laboratory Hematology;2011-02-22
5. Molecular basis and hematological features of hemoglobin variants in Southern Thailand;International Journal of Hematology;2010-09-14
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