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Hemoglobin
international journal for hemoglobin research
Volume 11, 1987 - Issue 6
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Original Article

Hyperunstable Hemoglobin Toyama [α2136(H19)LEU→ARGβ2]: Detection and Identification by in Vitro Biosynthesis with Radioactive Amino Acids

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Pages 539-556 | Received 04 Aug 1986, Accepted 11 Jul 1987, Published online: 07 Jul 2009

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Read on this site (12)

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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P. J. Ho, J. Rochette, D. C. Rees, C. A. Fisher, E. R. Huehns, A. M. Will & S. L. Thein. (1996) Hb Sun Prairie: Diagnostic Pitfalls in Thalassemic Hemoglobinopathies. Hemoglobin 20:2, pages 103-112.
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J. T. Prchal, B. Adler, J. B. Wilson, E. Baysal, W.-B. Qin, T. P. Molchanova, D. D. Pobedimskaya, E. G. Kazanetz & T. H. J. Huisman. (1995) HB Bibba OR α2136(H19)LEU→PROβ2 in a Caucasian Family from Alabama. Hemoglobin 19:3-4, pages 151-164.
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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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. (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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Articles from other publishers (3)

Andreas E. Kulozik. 2006. Pediatric Hematology. Pediatric Hematology 231 254 .
H. Wajcman, C. Vasseur, Y. Blouquit, J. Rosa, D. Labie, A. Najman, O. Reman, M. Leporrier & F. Galacteros. (1993) Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly). American Journal of Hematology 42:4, pages 367-374.
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H. Wajcman, V. Baudin‐Chich, J. Kister, C. Feo, G. Gombaud‐Saintonge, B. Bohn, M. Marden, J. Pagnier, C. Poyart, C. Dodé, F. Galacteros, Y. Blouquit, T. Cynober & G. Tchernia. (2006) Hemoglobin J Guantanamo [α 2 β 2 128 (H6) Ala→Asp] in association with hemoglobin C and α‐thalassemia in a family from Benin . American Journal of Hematology 28:3, pages 170-175.
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