References
- Chehab F. F., Der Kaloustian V., Khouri F. P., Deeb S. S., Kan Y. W. The molecular basis of β‐thalassemia in Lebanon: application of prenatal diagnosis. Blood 1987; 69: 1141–1145
- Zahed L., Talhouk R., Saleh M., Abou‐Jaoudeh R., Fisher C., Old J. M. The spectrum of β‐thalassemia mutations in the Lebanon. Hum. Hered. 1997; 47: 241–249
- Qatanani M., Taher A., Koussa S., Naaman R., Fisher C., Rugless M., Old J., Zahed L. β‐Thalassaemia intermedia in Lebanon. Eur. J. Haematol. 1999; 63: 1–8
- Varawalla N. Y., Old J. M., Weatherall D. J. Rare β‐thalassaemia mutations in Asian Indians. Br. J. Haematol. 1991; 79: 640–644
- Varawalla N. Y., Fitches A. C., Old J. M. Analysis of β‐globin gene haplotypes in Asian Indians: origin and spread of β‐thalassemia on the Indian subcontinent. Hum. Genet. 1992; 90: 443–449
- Venkatesan R., Sarkar R., Old J. M. β‐Thalassemia mutations and their linkage to β‐haplotypes in Tamilnadu in Southern India. Clin. Genet. 1992; 42: 251–256
- Rafie L., Rafie J. J. Thalassemia in Lebanon. 1984, International Red Cross Report
- Orkin S. H., Kazazian H. H., Jr., Antonarakis S. E., Goff S. C., Boehm C. D., Sexton G. D., 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
- Flint J., Harding R. M., Clegg J. B., Boyce A. J. Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants. Hum. Genet. 1993; 91: 91–117
- Flint J., Harding R. M., Boyce A. J., Clegg J. B. The population genetics of the haemoglobinopathies. Sickle Cell Disease and Thalassaemia, G. R. Rodgers. Bailliére's Clinical Haematology, Churchill Livingstone, LondonEngland 1998; Vol. 11: 1–51
- Bennani C., Bouhass R., Perrin‐Pecontal P., Tamouza R., Malou M., Elion J., Trabuchet G., Beldjord C., Benabadji M., Labie D. Anthropological approach to the heterogeneity of β‐thalassemia mutations in Northern Africa. Hum. Biol. 1994; 66: 369–382
- Rund D., Cohen T., Filon D., Dowling C. E., Warren T. C., Barak I., Rachmilewitz E., Kazazian H. H., Jr., Oppenheim A. Evolution of a genetic disease in an ethnic isolate: β‐thalassemia in the Jews of Kurdistan. Proc. Natl. Acad. Sci. USA 1991; 88: 310–314
- Gupta R. B., Tiwary R. S., Pande P. L., Kutlar F., Öner C., Öner R., Huisman T. H.J. Hemoglobinopathies among the Gond tribal groups of central India: interactions of α‐ and β‐thalassemia with β chain variants. Hemoglobin 1991; 15: 441–458
- Bandyopadhyay A., Bandyopadhyay S., Chowdhury M. D., Dasgupta U. B. Major β‐globin gene mutations in eastern India and their associated haplotypes. Hum. Hered. 1999; 49: 232–235
- Baysal E., Carver M. F.H. The β‐ and δ‐thalassemia repository (eighth edition). Hemoglobin 1995; 19: 213–236