REFERENCES
- http://globin.bx.psu.edu/Hbvar/menu.html (accessed September 2012).
- Wajcman H, Traeger-Synodinos J, Papassotiriou I, . Unstable and thalassemic α chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia. Hemoglobin. 2008; 32(4):327–349.
- Van Delft P, Lenters E, Bakker-Verweij M, . Evaluating five dedicated automatic devices for hemoglobinopathy diagnostics in multi ethnic populations. Int J Lab Hematol. 2009;31(5):484–495.
- Carrell RW, Kay RA. A simple method for the detection of unstable haemoglobin. Br J Hematol. 1972;23(5):615–619.
- 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.
- Sansone G, Sciarratta GV, Ivaldi G, Chiappara G. Hb H-like inclusions in red cells of patients with unstable haemoglobin. Haematologica. 1987;72(6):481–486.
- Brennan SO, Chan T, Sheen C. Novel hemoglobin (Hb Grey Lynn) substitution (α91 Leu→Phe ) affects heme interaction and α1β2 contacts. Clin Chem. 2007;53(5):990–991.
- Gallivan M. Ref ID 2619 (A-9986-2010), 2007 in http://globin.bx.psu.edu/Hbvar/menu.html.
- Brennan SO, Tauro GP, Melrose W. Hemoglobin Port Phillip α91 (FG3) Leu→Pro, a new unstable haemoglobin. FEBS Lett. 1977;81(1):115–117.
- Moradkhani K, Préhu C, Old J, . Mutation in the paralogous human α-globin genes yielding identical hemoglobin variants. Ann Hematol.2009;88(6):535–543.