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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 2
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Original Article

Hehoglobin Brest [β127(H5)Gln→LYS] a new Unstable Human Hemoglobin Variant Located at the α1β1 Interface with Specific Electrophoretic Behavior

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Pages 179-188 | Received 28 Aug 1987, Accepted 11 Dec 1987, Published online: 07 Jul 2009

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Päivikki Kangastupa, Kari Åkerman, Sari Risku, Matti Väisänen, Rutta Kuusela, Jarkko Romppanen, Annika Kouki, Mia Sneck, Outi Itkonen & Onni Niemelä. (2023) The prevalence of hemoglobin Tacoma in Finland detected by HbA1c capillary electrophoresis. Scandinavian Journal of Clinical and Laboratory Investigation 83:1, pages 51-57.
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Huan-Qing Chen, Li-Sha Wu, Fan Jiang & Dong-Zhi Li. (2021) Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case Report. Hemoglobin 45:5, pages 329-331.
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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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P. F. Como, D. R. Hocking, G. W. Swinton, R. J. Trent, R. A.B. Holland, E. A. Tibben, T. Wilkinson & H. Kronenberg. (1991) HB Geelong [β139(H17)ASN→ASP]. Hemoglobin 15:1-2, pages 85-95.
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. (1990) International Hemoglobin Information Center. Hemoglobin 14:3, pages 249-325.
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L. Kéclard, A. Campier, G. Mérault, A. Aupérin, J. Riou, J. Rosa & F. Galactéros. (1990) Hemoglobin Nevers [αβ2 130(H8)TYR↣R]; A New Silent Variant Found in France. Hemoglobin 14:1, pages 103-107.
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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 (1)

E. Girodon, N. Ghanem, M. Vidaud, J. Riou, J. Martin, F. Galactéros & M. Goossens. (1992) Rapid molecular characterization of mutations leading to unstable hemoglobin β-chain variants. Annals of Hematology 65:4, pages 188-192.
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