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Hemoglobin
international journal for hemoglobin research
Volume 1, 1977 - Issue 8
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Original Article

An Evaluation of the Methods for Quantitation of Hemoglobin A2; Results from a Survey of 10,663 Cases

Pages 845-860 | Received 25 Apr 1977, Accepted 23 Aug 1977, Published online: 07 Jul 2009

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Read on this site (5)

B. Chami, Y. Blouquit, J. Bardakdjian-Michau, J. Riou, H. Wajcman, J. Rosa & F. Galactéros. (1994) Hemlobin Variants in North Africa. Hemoglobin 18:1, pages 39-51.
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G. D. Efremov. (1992) Special Feature Hemoglobinopathies in Yugoslavia: an Update. Hemoglobin 16:6, pages 531-544.
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G. V. Sciarratta, G. Ivaldi, G. Sansone & P. Di Pietro. (1985) Hb 0-Arab [β121 (Gh4) Glu→Lys] in Italy. Hemoglobin 9:5, pages 513-515.
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. (1982) Hemoglobinopathies in Yugoslavia. Hemoglobin 6:6, pages 643-651.
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D. Bajanic, V. Oberiter, G. D. Efremov & T. H. J. Huisman. (1978) Hb Beograd (α2β2 121 (GH4) Glu → Val) Observed In A New Yugoslavian Family. Hemoglobin 2:5, pages 453-455.
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Articles from other publishers (14)

Pranee Winichagoon, Saovaros Svasti, Thongperm Munkongdee, Wantana Chaiya, Piatip Boonmongkol, Nawarath Chantrakul & Suthat Fucharoen. (2008) Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system. Translational Research 152:4, pages 178-184.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Ronald L. Nagel, Rajagopal Krishnamoorthy, Slaheddine Fattoum, Jacques Elion, Nathalie Genard, Jose Romero & Mary E. Fabry. (1999) The erythrocyte effects of haemoglobin OARAB. British Journal of Haematology 107:3, pages 516-521.
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Sherri A. Zimmerman, Erin E. O'Branski, Wendell F. Rosse & Russell E. Ware. (1999) Hemoglobin S/OARAB: Thirteen new cases and review of the literature. American Journal of Hematology 60:4, pages 279-284.
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Suthat Fucharoen, Pranee Winichagoon, Raewadee Wisedpanichkij, Busara Sae-Ngow, Rungrat Sriphanich, Warangkana Oncoung, Wanna Muangsapaya, Jew Chowthaworn, Sujin Kanokpongsakdi, Ahnond Bunyaratvej, Anong Piankijagum & Chris Dewaele. (1998) Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC. Clinical Chemistry 44:4, pages 740-748.
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P I Motum, A Kearney, T J Hamilton & R J Trent. (1993) Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.. Journal of Medical Genetics 30:3, pages 240-244.
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Penelope I. Motum, Robert Lindeman, Tracey J. Hamilton & Ronald J. Trent. (2008) Australian β 0 ‐thalassaemia: a high haemoglobin A 2 β 0 ‐thalassaemia due to a 12 kb deletion commencing 5′to the β‐globin gene . British Journal of Haematology 82:1, pages 107-113.
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Faouzi Baklouti, Alain Francina, Evelyne Dorléac, Véronique Baudin-Chich, Germaine Gombaud-Saintonge, Henri Plauchu, Henri Wajcman, Jean Delaunay & Jacqueline Godet. (1988) Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O-Arab (β121[GH4]Glu→Lys) in a Moroccan man. American Journal of Hematology 27:4, pages 253-256.
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J M White, M Byrne, R Richards, T Buchanan, E Katsoulis & K Weerasingh. (1986) Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia.. Journal of Medical Genetics 23:3, pages 245-251.
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J M White, R Richards, M Byrne, T Buchanan, Y S White & G Jelenski. (1985) Thalassaemia trait and pregnancy.. Journal of Clinical Pathology 38:7, pages 810-817.
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Eliezer A. Rachmilewitz, Hanna Tamari, Fanny Liff, Yoshihiro Ueda & R. L. Nagel. (2004) The interaction of hemoglobin O Arab with Hb S and β+ thalassemia among Israeli Arabs. Human Genetics 70:2, pages 119-125.
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P. Basset, F. Braconnier & J. Rosa. (1982) An update on electrophoretic and chromatographic methods in the diagnosis of hemoglobinopathies. Journal of Chromatography B: Biomedical Sciences and Applications 227:2, pages 267-304.
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W. A. Schroeder, Joan B. Shelton, J. Roger Shelton, Darleen Powars, Shlomo Friedman, James Baker, Jerry Z. Finklestein, B. Miller, Cage S. Johnson, J. R. Sharpsteen, Lance Sieger & Eric Kawaoka. (1982) Identification of eleven human hemoglobin variants by high-performance liquid chromatography: Additional data on functional properties and clinical expression. Biochemical Genetics 20:1-2, pages 133-152.
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C. Kattamis, A. Metaxotou‐Mavromati, W. G. Wood, J. R. Nash & D. J. Weatherall. (2008) The Heterogeneity of Normal Hb A 2 ‐β Thalassaemia in Greece . British Journal of Haematology 42:1, pages 109-123.
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