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Hemoglobin
international journal for hemoglobin research
Volume 6, 1982 - Issue 3
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Miscellaneous Article

International Hemoglobin Information Center Policies - IHIC

Pages 257-346 | Published online: 07 Jul 2009

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D. Juricic, I. Crepinko, G. D. Efremov, H. Lam, B. B. Webber, M. G. Headlee & T. H. J. Huisman. (1983) Hb A2-Zagreb Or α2δ2125(H3)Gln→Lglu, A New δ Chain Variant in Association with δβ-Thalassemia. Hemoglobin 7:5, pages 443-448.
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C. Romero Garcia, J. L. Navarro, H. Lam, B. B. Webber, M. G. Headlee, J. B. Wilson & T. H. J. Huisman. (1983) Hb A2-Manzanares Or α2δ2 121(Gh4) Glu→Val, An Unstable δ Chain Variant Observed in a Spanish Family. Hemoglobin 7:5, pages 435-442.
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Articles from other publishers (6)

Gianfranco Cossu, Mario Manca, Pier Giorgio Righetti, Elisabetta Gianazza, VÉRonique Baudin, Henri Wajcman & Adriana Bianchi‐Bosisio. (2005) Detection of neutral amino acid mutations by immobilized pH gradients: The case of the Tγ variant in fetal hemoglobin Sardinia. ELECTROPHORESIS 7:5, pages 213-216.
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Winston F. Moo-Penn, Danny L. Jue, Mary H. Johnson, Melisenda J. McDonald, Susan M. Turci, Tsu-Bi Shih, Richard T. Jones, Bradford L. TherrellJrJr & Arthur Arnone. (1984) Structural and functional studies of Hemoglobin Wayne: An elongated α-chain variant. Journal of Molecular Biology 180:4, pages 1119-1140.
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. (1983) Molecular Heterogeneity of Inherited Antithrombin III Deficiency. New England Journal of Medicine 309:17, pages 1063-1065.
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John R. Strahler, Barnett B. Rosenbloom & Samir M. Hanash. (1983) A Silent, Neutral Substitution Detected by Reverse-Phase High-Performance Liquid Chromatography: Hemoglobin Beirut. Science 221:4613, pages 860-862.
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Titus H. J. Huisman. (2006) Percentages of abnormal hemoglobins in adults with a heterozygosity for an α‐chain and/or a β‐chain variant. American Journal of Hematology 14:4, pages 393-404.
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Teruo Harano, Keiko Harano, Susumu Shibata, Satoshi Ueda, Hiroo Mori & Naomichi Arimasa. (1983) Hemoglobin Okayama [β-2 (NA 2) His → Gln]: A new ‘silent’ hemoglobin variant with substituted amino acid residue at the 2,3-diphosphoglycerate binding site. FEBS Letters 156:1, pages 20-22.
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