HETEROGENEITY OF MESSENGER RNA DEFECTS IN THE THALASSEMIA SYNDROMES
- 1 May 1980
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 344 (1) , 101-112
- https://doi.org/10.1111/j.1749-6632.1980.tb33653.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Proteolytic activity in erythrocyte precursorsProceedings of the National Academy of Sciences, 1978
- Characterization of β-globin mRNA in the β0 thalassemiasCell, 1978
- Variability in the amount of β-globin mRNA in β0 thalassemiaCell, 1978
- Regulation of Hemoglobin Synthesis during the Development of the Red CellNew England Journal of Medicine, 1977
- Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.Proceedings of the National Academy of Sciences, 1977
- Globin Synthesis During Erythroid Cell Maturation in α ThalrssemiaHemoglobin, 1976
- Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.Journal of Clinical Investigation, 1975
- Globin Messenger RNA in Hemoglobin H DiseaseBlood, 1973
- Quantitative Deficiency of Chain-Specific Globin Messenger Ribonucleic Acids in the Thalassemia SyndromesProceedings of the National Academy of Sciences, 1973
- Haemoglobin Synthesis during Erythroid Maturation in β-ThalassaemiaNature New Biology, 1972