THE POTENTIAL MOLECULAR MECHANISM OF THALASSEMIAS AND RELATED DISORDERS
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1974.tb21873.x/fullpdf
Reference35 articles.
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3. The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-Thalassaemia
4. 5. Fessas, P. Proc. XXI Cong. Int. Soc. Haematol. : 52 .
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. Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemia.;Journal of Biological Chemistry;1990-10
2. Hereditary Anemias of the Mouse: A Review for Geneticists;Advances in Genetics;1979
3. The molecular basis of the thalassemia syndromes;Japanese journal of human genetics;1977-09
4. Multiple hemoglobin α-chains in the sika deer (Cervus nippon);Biochimica et Biophysica Acta (BBA) - Protein Structure;1977-05
5. Specific radioimmunochemical identification and quantitation of hemoglobins a2 and f;American Journal of Hematology;1976
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