References
- Baysal E., Carver M. F.H. The β‐ and δ‐thalassemia repository (eighth edition). Hemoglobin 1995; 19: 213–236
- Newton C. R., Graham A., Heptinstall L. E., Powell S. J., Summers C., Kalshekar N., Smith J. C., Markham A. E. Analysis of any point mutation in DNA: the amplification refractory mutation system (ARMS). Nucleic Acids Res. 1989; 17: 2503–2516
- Old J. M., Varawalla N. Y., Weatherall D. J. Rapid detection and prenatal diagnosis of β‐thalassaemia: studies in Indian and Cypriot populations in the UK. The Lancet 1990; 336: 834–837
- Losekoot M., Fodde R., Harteveld C. L., Heeren H. V., Giordano P. C., Went L. N., Bernini L. F. Homozygous β+ thalassemia owing to a mutation in the cleavage‐polyadenyl‐ation sequence of the human β globin gene. J. Med. Genet. 1991; 28: 252–255
- Ghanem N., Girodon E., Vidaud M., Martin J., Fanen P., Plassa F., Goossens M. A comprehensive scanning method for rapid detection of β‐globin gene mutations and polymorphisms. Hum. Mut. 1992; 1: 229–239