A Novel Frameshift Mutation [FSC 47 (+A)] Causing β-Thalassemia in a Surinam Patient
- 1 January 1990
- journal article
- Published by Taylor & Francis in Hemoglobin
- Vol. 14 (4) , 467-470
- https://doi.org/10.3109/03630269009032010
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.Proceedings of the National Academy of Sciences, 1989
- Molecular basis and prenatal diagnosis of beta-thalassemiaBlood, 1988
- [31] Detection and localization of single base changes by denaturing gradient gel electrophoresisPublished by Elsevier ,1987
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986