Globin Chain Synthesis in β-Thalassemia with Normal Hemoglobins A2and F
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630267908996902
Reference6 articles.
1. Different Types of Beta-Thalassemia Intermedia
2. Abnormal human haemoglobins
Cited by 7 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. β + Thalassaemia-Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia;British Journal of Haematology;2008-07-07
2. Genetic and Molecular Analysis of Mild Forms of Homozygous ?-Thalassemia;Annals of the New York Academy of Sciences;1985-06
3. β+Thalassaemia—Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia;British Journal of Haematology;1983-06
4. Effect of Transferrin Absence on in Vitro Globin Chain Synthesis in Reticulocytes of β-Thalassemic Patients;Hemoglobin;1983-01
5. β-Thalassemia intermedia Homozygous for Normal Hemoglobin A2 β-Thalassemia;Acta Haematologica;1982
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