REFERENCES
- Old J. M., Varawalla N. Y., Weatherall D. J. Rapid detection and prenatal diagnosis of β-thalassaemia: studies in the Indian and Cypriot populations of the UK. The Lancet 1990; 336: 834–837
- Saiki R. K., Gelfand D. H., Stoeffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 1998; 239: 487–491
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain termination inhibitors. Proc. Natl. Acad. Sci. USA 1977; 74: 5463–5467
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 1975; 98: 503–517
- Huisman T. H.J., Carver M. F.H., Baysal E. A Syllabus of Thalassemia Mutations (1997). The Sickle Cell Anemia Foundation, Augusta, GAUSA 1997, (http: //globin.cse.psu.edu)
- Sheets M. D., Ogg S. C., Wickens M. P. Point mutations in AAUAAA and the poly (A) addition Site: effects on the accuracy and efficiency of cleavage and polyadenyla-tion in vitro. Nucleic Acids Res. 1990; 18: 5799–5805