Characterization of the B+-Thalassemia Mutation in a Homozygous Yugoslavian Patient
- 1 January 1984
- journal article
- case report
- Published by Taylor & Francis in Hemoglobin
- Vol. 8 (5), 529-534
- https://doi.org/10.3109/03630268408991739
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Dutch β°‐thalassaemia: a 10 kilobase DNA deletion associated with significant γ‐chain productionBritish Journal of Haematology, 1984
- THE MOLECULAR BASIS FOR β° THALASSAEMIA INTERMEDIA IN AN IRANIAN INDIVIDUALBritish Journal of Haematology, 1982
- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982
- The nucleotide sequence of the human β-globin geneCell, 1980
- Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.Proceedings of the National Academy of Sciences, 1979