REFERENCES
- Huisman T. H.J., Carver M. F.H., Baysal E. A Syllabus of Thalassemia Mutations (1997). The Sickle Cell Anemia Foundation, Augusta, GA, USA 1997, (http://globin.cse.psu.edu)
- Fullerton S., Clegg J. B. HpaI, HindIII and BamHI polymorphisms 3′ of the human β-globin gene can be detected by a single polymerase chain reaction amplification product. Am. J. Hematol. 1994; 47: 256
- Kulozik A. E., Lyons J., Kohne E., Bartram C. R., Kleihauer E. Rapid and non-radioactive prenatal diagnosis of β thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR). Br. J. Haematol. 1988; 70: 455–458
- Orkin S. H., Kazazian H. H., Jr., Antonarakis S. E., Goff S. C., Boehm C. D., Sexton J. P., Waber P. G., Giardina P. J.V. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature 1982; 296: 627–631
- Wajcman H., Kilmartin J. V., Najman A., Labie D. Hemoglobin Cochin-Port Royal: consequences of the replacement of the β chain C-terminal by an arginine. Biochim. Biophys. Acta 1975; 400: 354–364
- Arnone A., Gacon G., Wajcman H. X-ray and functional studies of Hemoglobins Nancy and Cochin-Port Royal. J. Biol. Chem. 1976; 251: 5875–5880