The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-Thalassaemia
- 1 March 1969
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 16 (3), 251-268
- https://doi.org/10.1111/j.1365-2141.1969.tb00400.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Haemoglobin Synthesis in β-ThalassaemiaNature, 1968
- Hemoglobin synthesis in β-thalassemia: the properties of the free α-chainsJournal of Clinical Investigation, 1968
- Excess of α‐Globin Synthesis in Homozygous β‐Thalassemia and its Removal from the Red Blood Cell CytoplasmEuropean Journal of Biochemistry, 1968
- alpha-Chain and Globin: Intermediates in the Synthesis of Rabbit HemoglobinEuropean Journal of Biochemistry, 1967
- Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)Nature, 1967
- Haemoglobin synthesis in ThalassaemiaTransactions of the Royal Society of Tropical Medicine and Hygiene, 1967
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counterAnalytical Biochemistry, 1960
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine ContentJournal of the American Chemical Society, 1958