REFERENCES
- Bissé E, Wieland H. High-performance liquid chromatographic separation of human haemoglobins simultaneous quantitation of foetal and glycated haemoglobins. J Chromatogr. 1988;434(1):95–110.
- Kleinert P, Schmid M, Zurbriggen K, Mass spectrometry: a tool for enhanced detection of hemoglobin variants. Clin Chem. 2008;54(1):69–76.
- Kutlar F, Kutlar A, Huisman THJ. Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography. J Chromatogr. 1986;357(1):147–153.
- Basset P, Beuzard Y, Garel MC, Rosa J. Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins. Blood. 1978;51(5):971–982.
- Duc G, Engel K. A method for determination of oxyhemoglobin dissociation curves at constant temperature, pH, and PCO2. Respir Physiol. 1969;8(1):118–126.
- Globin Gene Server: http://globin.cse-psu.edu.
- Wajcman H, Elion J, Boissel JP, Labie D, Jos J, Girot R. A silent hemoglobin variant: Hemoglobin Necker Enfants-Malades α20(B1)His→Tyr. Hemoglobin. 1980;4(2):177–184.
- Fleming PJ, Sumner DR, Wyatt K, Hemoglobin Hobart or α20(Bl)His→Arg: a new α chain hemoglobin variant. Hemoglobin. 1987;11(3):211–220.
- Cotton F, Wajcman H, Hansen V, Hb Anderlecht [α20(B1)His→Pro]: a silent variant found in a Congolese newborn. Hemoglobin. 2000;24(4):299–304.
- Malcorra-Azpiazu JJ, Balda-Aguirre MI, Diaz-Chico JC, Hb Le Lamentin or α220(B1)His→Glnβ2 found in a Spanish family. Hemoglobin. 1988;12(2):201–205.
- Harano T, Harano K, Shibata S, Hb Le Lamentin [α20 (B1)His→Gln] in Japan: structure, function and biosynthesis. Hemoglobin. 1983;7(2):181–184.
- Wiener K, McFarlane X, Green BN. Increasing recognition of Haemoglobin Le Lamentin. J Clin Pathol. 2001;54(12):970.
- Reynolds TM, McMillan F, Smith A, Hutchinson, Green B. Haemoglobin Le Lamentin (α20(B1)His→Gln) in a British family: identification by electrospray mass spectrometry. J Clin Pathol. 1998;51(6):467–470.
- Sellaye M, Blouquit Y, Galacteros F, A new silent hemoglobin variant in a Black family from French West Indies, Hemoglobin Le Lamentin α20 His→Gln. FEBS Lett. 1982;145(1):128–130.
- Heaton DC, Fellowes AP, George PM. Concurrence of hereditary spherocytosis and α thalassaemia. Aust NZ J Med. 1991;21(4):485–486.
- Li CK, Ng MH, Cheung KL, Lam TK, Shing MM. Interaction of hereditary spherocytosis and α thalassaemia: a family study. Acta Haematol. 1994;91(4):201–205.
- Uysal Z, Yildirmak Y, Akar N, Başak N, Cin S. α-Thalassemia and hereditary spherocytosis in the same patient: the interaction of two diseases. Pediatr Hematol Oncol. 1998;15(3):271–276.