α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia
- 1 August 1979
- journal article
- Published by Springer Nature in Nature
- Vol. 280 (5723) , 605-607
- https://doi.org/10.1038/280605a0
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Frequencies of thalassemia in American blacksBlood, 1977
- Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at BirthPediatric Research, 1977
- Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural lociNature, 1975
- Relative numbers of human globin genes assayed with purified alpha and beta complementary human DNA.Proceedings of the National Academy of Sciences, 1975
- Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)Nature, 1974
- Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletionNature, 1974
- α-Thalassemia in the American NegroJournal of Clinical Investigation, 1972
- Multiple Alpha Chain Loci for Human Haemoglobins: Hb J-Buda and Hb G-PestNature, 1972
- The Thalassaemia Syndromes in NigeriaBritish Journal of Haematology, 1970
- Differences between - and -Chain Mutants of Human Haemoglobin and between - and -Thalassaemia. Possible Duplication of the -Chain GeneBMJ, 1968