THE CLINICAL AND CHEMICAL HETEROGENEITY OF THE β‐THALASSEMIAS
- 1 May 1974
- journal article
- review article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 232 (1) , 88-106
- https://doi.org/10.1111/j.1749-6632.1974.tb20575.x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Haemoglobin Synthesis during Erythroid Maturation in β-ThalassaemiaNature New Biology, 1972
- Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaJournal of Clinical Investigation, 1971
- Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytesJournal of Clinical Investigation, 1971
- Beta Thalassemia and Translation of Globin Messenger RNAProceedings of the National Academy of Sciences, 1971
- Heterozygous Beta Thalassemia: Balanced Globin Synthesis in Bone Marrow CellsScience, 1970
- Haemoglobin Synthesis in β-ThalassaemiaBritish Journal of Haematology, 1969
- Changing rates of globin chain synthesis during erythroid cell maturation in thalassemiaJournal of Molecular Biology, 1969
- The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-ThalassaemiaBritish Journal of Haematology, 1969
- Haemoglobin Synthesis in β-ThalassaemiaNature, 1968
- THE TURNOVER OF HEMOGLOBINS A, F, AND A2 IN THE PERIPHERAL BLOOD OF THREE PATIENTS WITH THALASSEMIA*Journal of Clinical Investigation, 1963