Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion
- 1 October 1974
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature
- Vol. 251 (5474), 389-392
- https://doi.org/10.1038/251389a0
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- HEMOGLOBIN CONSTANT SPRING, AN UNUSUAL α‐CHAIN VARIANT INVOLVED IN THE ETIOLOGY OF HEMOGLOBIN H DISEASEAnnals of the New York Academy of Sciences, 1974
- Quantitative Deficiency of Chain-Specific Globin Messenger Ribonucleic Acids in the Thalassemia SyndromesProceedings of the National Academy of Sciences of the United States of America, 1973
- IS THE HUMAN GLOBIN α‐CHAIN LOCUS DUPLICATED?British Journal of Haematology, 1973
- IQ Evoked Responses and Fourier AnalysisNature, 1973
- Haemoglobin Constant Spring—A Chain Termination Mutant ?Nature, 1971
- Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytesJCI Insight, 1971
- DIFFERENT TYPES OF ALPHA-THALASSÆMIA AND SIGNIFICANCE OF HÆMOGLOBIN BART'S IN NEONATESThe Lancet, 1970
- The Haemoglobin Constitution of Infants with the Haemoglobin Bart's Hydrops Foetalis SyndromeBritish Journal of Haematology, 1970
- Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)Nature, 1967
- Thalassemia: The consequences of unbalanced hemoglobin synthesisAmerican Journal Of Medicine, 1966