REFERENCES
- Morlé F, Francina A, Ducrocq R, . A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with Hb H disease in one homozygous patient. Br J Haematol. 1995;91(3):608–611.
- Khan SN, Butt FI, Riazuddin S, Galanello R. Hb Sallanches [α104(G11)Cys→Tyr]: a rare α2-globin chain variant found in the homozygous state in three members of a Pakistani family. Hemoglobin. 2000;24(1):31–35.
- Waye JS, Walker L, Chui DHK, Lafferty J, Kirby M. Homozygous Hb Sallanches [α104(G11)Cys→Tyr] in a Pakistani child with Hb H disease. Hemoglobin. 2000;24(4):355–357.
- Dash S, Harano K, Menon S. Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: an unstable hemoglobin variant found in an Indian child. Hemoglobin. 2006;30(3):393–396.
- Sarkar AA, Banerjee S, Chandra S, . A novel 33.3 kb deletion (− −KOL) in the α-globin gene cluster: a brief report on deletional α-thalassaemia in the heterogeneous eastern Indian population. Br J Haematol. 2005;130(3):454–457.
- Bhattacharya G, Sarkar AA, Banerjee D, Chandra S, Das M, Dasgupta UB. Polymerase chain reaction-based search for two α-globin gene mutations in India. Hemoglobin. 2008;32(5):485–490.
- Chan AY, So CK, Chan LC. Comparison of the Hb H inclusion test and a PCR test in routine screening for α thalassemia in Hong Kong. J Clin Pathol. 1996 May;49(5):411–413.
- Dodé C, Rochette J, Krishnamoorthy R. Locus assignment of human α globin mutations by selective amplification and direct sequencing. Br J Haematol.. 1990;76(2):275–281.
- Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol. 1994;46(3):208–213.
- Moradkhani K, Préhu C, Old J, . Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants. Ann Hematol. 2009;88(6):535–543.