A MODEL FOR THE PERSISTENCE OR REACTIVATION OF FETAL HqMOGLOBIN PRODUCTION
Authors:
- D J WeatherallDWD J Weatherall
- J B CleggJCJ B Clegg
- 1 September 1976
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 308 (7987) , 660-663
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- δβ-Thalassemia is due to a gene deletionCell, 1976
- Stimulation of fetal hemoglobin synthesis in bone marrow cultures from adult individuals.Proceedings of the National Academy of Sciences, 1976
- Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemiaJournal of Clinical Investigation, 1968
- THE TURNOVER OF HEMOGLOBINS A, F, AND A2 IN THE PERIPHERAL BLOOD OF THREE PATIENTS WITH THALASSEMIA*Journal of Clinical Investigation, 1963
- Alkali-Resistant Hemoglobin in Aplastic Anemia of Both Acquired and Congenital TypesNew England Journal of Medicine, 1962