References
- Higgs D. R., Vickers M. A., Wilkie A. O.M., Pretorius I. M., Jarman A. P., Weatherall D. J. A review of the molecular genetics of the human α‐globin gene cluster. Blood 1989; 73: 1081–1104
- Liebhaber S. A. α Thalassemia. Hemoglobin. 1989; 13: 685–731
- Southern E. M. Detection of specific sequences among fragments separated by gel electrophoresis. J. Mol. Biol. 1975; 98: 503–517
- Bowden D. K., Vickers M. A., Higgs D. R. A PCR‐based strategy to detect the common severe determinants of α‐thalassaemia. Br. J. Haematol. 1992; 81: 104–108
- Dodé C., Rochette J., Krishnamoorthy R. Locus assignment of human α‐globin gene mutations by selective amplification and direct sequencing. Br. J. Haematol. 1990; 76: 275–281
- Morlé F., Francina A., Ducrocq R., Wajcman H., Gonnet C., Philippe N., Souillet G., Godet J. A new a chain variant Hb Sallanches ‘α2 104(G11) Cys→Tyr’ associated with Hb H disease in one homozygous patient. Br. J. Haematol. 1995; 91: 608–611
- Préhu C., Préhu M. O., Privato M., Maisonneuve H., Bardakdjian J., Wajcman H., Goossens M., Galactéros F. Hb Sallanches (α 104(G 11 )Cys→Tyr) in association with an a‐3,7 kb deletion leads to Hb H disease. Br. J. Haematol. 1996; 93: 25, (suppl.)
- Kahn S. N., Butt F. I., Riazuddin S., Galanello R. Hb Sallanches ‘α 104(GI I)Cys → Tyr’: a rare α2–globin chain variant found in the homozygous state in three members of a Pakistani family. Hemoglobin 2000; 4: 31–35