REFERENCES
- Botha MC, Beale D, Isaacs WA, Lehmann H. Hemoglobin J Cape Town α292arginine→glutamineβ2. Nature 1966; 212(5064)792–795
- Jenkins T, Stevens K, Gallo E, Lehmann H. A second family possessing Haemoglobin J α Cape Town. S Afr Med J 1968; 42(42)1151–1154
- Botha MC, Stathopoulou R, Lehmann H, Rees JS, Plowman DA. A Hb J Cape Town homozygote—association of Hb J Cape Town and α-thalassaemia. FEBS Lett 1978; 96(2)331–334
- Jenkins T. Genetic polymorphisms of a man in Southern Africa. University of London. 1972, M.D. Thesis,
- Harano T, Harano K, Shibata S, Ueda S, Mori H, Imai K. Hb Chesapeake [α92 (FG 4) Arg→Leu] and Hb J Cape Town [α92 (FG 4) Arg→Gln] first discovered in Japanese. Hemoglobin 1983; 7(5)461–465
- Horiuchi T, Nakamura T, Tsutsumi H, Miyao M, Inoue J, Araki A, Hattori A, Harano A, Mori M, Ito H. A case of abnormal hemoglobin (HbJ Cape Town) with high serum levels of HbAlc. Nippon Ronen Igakkai Zasshi 1996; 33(2)110–115
- Harano T. Hemoglobinopathy in Japan: detection and analysis. Rinsho Byori 1999; 47(3)215–223
- Huisman THJ, Jonxis JHP. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis. Marcel Dekker, Inc., New York 1977; 6
- Carbone V, Salzano AM, Pagnini D, Papa G, Libertino R, Pagano L, De Rosa C, Pucci P. The mutation associated with Hb Peterborough [β111(G13)Val→Phe] originated from Southern Italy. Hemoglobin 2000; 24(3)227–237
- Carbone V, Salzano AM, Pagano L, Viola A, Buffardi S, De Rosa C, Pucci P. Hb Rainier [β145(HC2)Tyr→Cys] in Italy. Characterization of the amino acid substitution and the DNA mutation. Hemoglobin 1999; 23(2)111–124
- Salzano AM, Carbone V, Pagano L, Buffardi S, De RC, Pucci P. Hb Vila Real [β36(C2)Pro→His] in Italy: characterization of the amino acid substitution and the DNA mutation. Hemoglobin 2002; 26(1)21–31
- Foglietta E, Deidda G, Graziani B, Modiano G, Bianco I. Detection of α-globin gene disorders by a simple PCR methodology. Haematologica 1996; 81(5)385–386
- Prome D, Prome JC, Pratbernou F, Blouquit Y, Galacteros F, Lacombe C, Rosa J, Robinson JD. Identification of some abnormal hemoglobins by fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometry. Biomed Environ Mass Spectrom 1988; 16(1–12)41–44
- Dode C, Krishnamoorthy R, Lamb J, Rochette J. Rapid analysis of −α3.7thalassaemia and αααanti 3.7triplication by enzymatic amplification analysis. Br J Haematol 1993; 83(1)105–111
- Charache S, Jenkins T. Oxygen equilibrium of Hemoglobin J Cape Town. J Clin Invest 1971; 50(7)1554–1555
- Nagel RL, Gibson QH, Charache S. Relation between structure and function in Hemoglobin Chesapeake. Biochemistry 1967; 6(8)2395–2402
- Wajcman H, Kister J, A M'Rad, Soummer AM, Galacteros F. Hb Cemenelum [α92(FG4)Arg→Trp]: a hemoglobin variant of the α1/β2 interface that displays a moderate increase in oxygen affinity. Ann Hematol 1994; 68(2)73–76
- Clegg JB, Naughton MA, Weatherall DJ. Abnormal human haemoglobins. Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb-Chesapeake and Hb-J-Bangkok. J Mol Biol 1966; 19(1)91–108
- Charache S, Weatherall DJ, Clegg JB. Polycythemia associated with a hemoglobinopathy. J Clin Invest 1966; 45(6)813–822
- Pearson TC, Messinezy M, Westwood N, Green AR, Bench AJ, Green AR, Huntly BJ, Nacheva EP, Barbui T, Finazzi G. A polycythemia vera updated: diagnosis, pathobiology, and treatment. Hematology Am Soc Hematol Educ Program. 2000; 51–68