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Hemoglobin
international journal for hemoglobin research
Volume 8, 1984 - Issue 3
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Original Article

The Association of Hemoglobin Knossos and Hemoglobin Lepore in an Algerian Patient

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Pages 229-238 | Received 24 Oct 1983, Accepted 16 Jan 1984, Published online: 07 Jul 2009

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Read on this site (5)

Eunice Sindhuvi Edison, Ramachandran V. Shaji, Alok Srivastava & Mammen Chandy. (2005) Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls. Hemoglobin 29:3, pages 221-224.
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A. Kutlar, F. Kutlar, M. Aksoy, A. Gurgey, Ç. Altay, J. B. Wilson, J. C. Diaz-Chico, H. Hu & T. H. J. Huisman. (1989) β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia. Hemoglobin 13:1, pages 7-16.
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Pratumtip Boontrakoonpoontawee, Jisnuson Svasti, Suthat Fucharoen & Pranee Winichagoon. (1987) Identification of HB Lepore-Mashington-Boston in Association with HB E [βB26(B8)GLU→LYS] in a Thai Female. Hemoglobin 11:4, pages 309-316.
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S. El Wan, F. Baklouti, M. El-Kabsh, F. Abdelrahman & J. Delaunay. (1987) Hemoglobin Knossos [α2β227(B9)Ala →] in Egypt. Hemoglobin 11:2, pages 139-143.
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A. Francina, S. Elwan, F. Baklouti, J. Delaunay, E. Dorleac, M. Aubry, L. Roda & N. Phillipe. (1985) Hb Lepore-Hb C and Hb Lepore-β°-Thalassemia Compound Heterozygotes1 N an Algerian Family. Hemoglobin 9:5, pages 505-508.
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Articles from other publishers (9)

Ibrahim KeserEsra ManguogluOzlem KayisliAkif YesilipekGuven Luleci. (2007) Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major. Genetic Testing 11:3, pages 228-230.
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Vip Viprakasit, Parichat Pung‐Amritt, Lerlugh Suwanthon, Kevin Clark & Voravarn S. Tanphaichitr. (2002) Complex interactions of δβ hybrid haemoglobin (Hb Lepore‐Hollandia) Hb E (β 26 G→A ) and α + thalassaemia in a Thai family . European Journal of Haematology 68:2, pages 107-111.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
George Vassilopoulos, Ioannis Papassotiriou, Ersi Voskaridou, Alexandra Stamoulakatou, Evangelos Premetis, Jean Kister, Michael Marden, Nathalie Griffon, Claude Poyart, Henri Wajcman, Frederic Galacteros & Dimitris Loukopoulos. (2008) Hb Arta [β45 (CD4) Phe→Cys]: a new unstable haemoglobin with reduced oxygen affinity in trans with β‐thalassaemia. British Journal of Haematology 91:3, pages 595-601.
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John S. Waye, Barry Eng, Margaret Patterson, David H. K. Chui, Lebe S. Chang, Bessie Cogionis, Annette O. Poon & Nancy F. Olivieri. (2006) Hb E/Hb Lepore Hollandia in a family from Bangladesh . American Journal of Hematology 47:4, pages 262-265.
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R. J. Olds, T. Sura, B. Jackson, B. Wonke, A. V. Hoffbrand & S. L. Thein. (1991) A novel δº mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families. British Journal of Haematology 78:3, pages 430-436.
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R. Ouazana, D. Bozon, F. Baklouti, C. Gonnet, J. Delaunay & J. Godet. (2001) δ°‐Thalassemia in cis of β Knossos ‐globin gene Normal structure and normal transient expression of the δ‐globin gene . FEBS Letters 252:1-2, pages 53-57.
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L. Oggiano, M. Pirastu, P. Moi, M. Longinotti, L. Perseu & A. Cao†. (2008) Molecular characterization of a normal Hb A 2 β‐thalassaemia determinant in a Sardinian family . British Journal of Haematology 67:2, pages 225-229.
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Phaedon Fessas, Dimitris Loukopoulos, Stavroula Kokkinou, Yannis Papasotiriou & Aris Karaklis. (2006) Hemoglobin knossos: A clinical, laboratory, and epidemiological study. American Journal of Hematology 21:2, pages 119-133.
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