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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 1
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Original Article

Interaction of Hemoglobin Siriraj with Hemoglobin S: A Mild Sickle Cell Syndrome

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Pages 21-31 | Received 16 Jul 1985, Accepted 04 Nov 1965, Published online: 07 Jul 2009

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J. Földi, M. Horányi, J.G. Szelényi, S. R. Hollán, E. A. Aseeva, I. N. Lutsenko, V. A. Spivak, O. Tóth & B. V. Rozynov. (1989) Hemoglobin Siriraj Found in the Hungarian Population. Hemoglobin 13:2, pages 177-180.
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Articles from other publishers (5)

Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 185 260 .
Titus Hendrik Jan Huisman. (1997) Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations: influence on phenotype. Clinical Chemistry 43:10, pages 1850-1856.
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Sophie Lesecq, Véronique Baudin, Jean Kister, Michael C. Marden, Claude Poyart & Josée Pagnier. (1996) Functional Studies and Polymerization of Recombinant Hemoglobin Glu-α2β26(A3) → Val/Glu-7(A4) → Ala. Journal of Biological Chemistry 271:29, pages 17211-17214.
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K. Adachi, L.R. Reddy & S. Surrey. (1994) Role of hydrophobicity of phenylalanine beta 85 and leucine beta 88 in the acceptor pocket for valine beta 6 during hemoglobin S polymerization.. Journal of Biological Chemistry 269:50, pages 31563-31566.
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D.J. Yamashiro, M. Adachi, P. Konitzer, S. Surrey & K. Adachi. (1994) Polymerization and instability of a recombinant hemoglobin containing valine beta 7.. Journal of Biological Chemistry 269:39, pages 23996-23999.
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