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Hemoglobin
international journal for hemoglobin research
Volume 8, 1984 - Issue 2
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Original Article

The Characterization of Hemoglobin Manitoba or α2102(G9)Ser→Argβ2 and Hemoglobin Contaldo or α2103(G10)HIS→ARGβ2 By High Performance Liquid Chromatography

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Pages 169-181 | Received 10 Jan 1984, Accepted 31 Jan 1984, Published online: 07 Jul 2009

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Mohamed S.M. Khalil, Adele T. Timbs, Shirley J. Henderson, Anna Schuh & John M. Old. (2020) Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression. Hemoglobin 44:6, pages 442-445.
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Beverley M. Pullon & Jordyn A. Moore. (2020) Hb Manitoba [α102(G9)Ser→Arg] in Pasifika: Tongan Case Report. Hemoglobin 44:4, pages 290-293.
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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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James D. Hoyer, Daniel J. McCormick, Karen Snow, Jong H. Kwon, David Booth, Manuel Duarte, Guy Grayson, Kathleen S. Kubik, Michael W. Holmes & Virgil F. Fairbanks. (2002) FOUR NEW VARIANTS OF THE α2-GLOBIN GENE WITHOUT CLINICAL OR HEMATOLOGIC EFFECTS: Hb PARK RIDGE [α9(A7)Asn→Lys (α2)], Hb NORTON [α72(EF1)His→Asp (α2)], HbLOMBARD [α103(G10)His→Tyr (α2)], AND Hb SAN ANTONIO [α113(GH2)Leu→Arg (α2)]. Hemoglobin 26:2, pages 175-180.
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Jan-Gowth Chang, Mu-Chin Shih, Su-Ching Liu, Wen-Ling Chan & Ching-Tien Peng. (2001) Hb MANITOBA IN A TAIWANESE FAMILY: A C → A SUBSTITUTION AT CODON 102 OF THE α2-GLOBIN GENE. Hemoglobin 25:4, pages 437-439.
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P. Lacan, A. Francina, G. Souillet, M. Aubry, N. Couprie, L. Dementhon & M. Becchi. (1999) Two New α Chain Variants: Hb Boghé [α58(E7)His→Gln, α2], a Variant on the Distal Histidine, and Hb Charolles [α03(G10)His→Tyr, α1]. Hemoglobin 23:4, pages 345-352.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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Y. Ohba. (1990) Unstable Hemoglobins. Hemoglobin 14:4, pages 353-388.
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. (1990) International Hemoglobin Information Center. Hemoglobin 14:3, pages 249-325.
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G. V. Sciarratta & G. Ivaldi. (1990) Hb Hatera [β55(D6)Met↣Lys]: A new Unstable Hemoglobin Variant in an Italian Family. Hemoglobin 14:1, pages 79-85.
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. (1989) Variants of the Alpha Chain. Hemoglobin 13:3, pages 223-297.
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. (1988) IHIC Variants List. Hemoglobin 12:3, pages 209-282.
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. (1987) IHIC Variants List. Hemoglobin 11:3, pages 243-308.
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. (1985) International Hemoglobin Information Center. Hemoglobin 9:3, pages 229-298.
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Articles from other publishers (3)

Steven Dajnowicz, Sean Seaver, B. Leif Hanson, S. Zoë Fisher, Paul Langan, Andrey Y. Kovalevsky & Timothy C. Mueser. (2016) Visualizing the Bohr effect in hemoglobin: neutron structure of equine cyanomethemoglobin in the R state and comparison with human deoxyhemoglobin in the T state. Acta Crystallographica Section D Structural Biology 72:7, pages 892-903.
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Xiang YuTodd L. MollanAndrew Butler, Andrew J. Gow, John S. OlsonMitchell J. Weiss. (2009) Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein. Blood 113:23, pages 5961-5969.
Crossref
Corinne Vasseur-Godbillon, Michael C. Marden, Piero Giordano, Henri Wajcman & Véronique Baudin-Creuza. (2006) Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells, Molecules, and Diseases 37:3, pages 173-179.
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