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Shohreh Khatami, Soghra Rouhi Dehboneh, Sedigheh Sadeghi, Roghieh Mirzazadeh, Parinaz Saeedi, Parastoo Bayat, Hossein Najmabadi, Sirous Zeinali, Mohammad Taghi Akbari, Mohammad Ardjmand & Aref Amirkhani. (2007) Globin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias. Hemoglobin 31:3, pages 333-341.
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Roghieh Mirzazadeh, Shohreh Khatami, Parastoo Bayat, Zahra Zamani, Sedigheh Sadeghi, Soghra Roohi & Parinaz Saidi. (2005) Removing Peroxide Impurities from Ether Improves the Quality of Globin Chains for Biosynthetic Studies. Hemoglobin 29:2, pages 161-164.
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Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2001) Hb GERLAND [α55(E4)Val → Ala (α2)]: A NEW NEUTRAL α CHAIN VARIANT INVOLVING THE α2 GENE. Hemoglobin 25:4, pages 417-420.
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P. Lacan, A. Francina, G. Souillet, M. Aubry, N. Couprie, L. Dementhon & M. Becchi. (1999) Two New α Chain Variants: Hb Boghé [α58(E7)His→Gln, α2], a Variant on the Distal Histidine, and Hb Charolles [α03(G10)His→Tyr, α1]. Hemoglobin 23:4, pages 345-352.
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P. Lacan, M. Aubry, A. Francina, N. Couprie, L. Dementhon & M. Becchi. (1999) Characterization of Hb djeifa [β98(FG5)Val→Ala] by DNA sequencing in a French caucasian family. Hemoglobin 23:1, pages 73-77.
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P. Lacan, M. Aubry, A. Francian & A. Lachaux. (1997) HB Zengcheng [β114(G16)LEU→MET] in a Cambodian Family. Hemoglobin 21:4, pages 363-367.
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P. Lacan, A. Francina, D. Prome, J. Delaunay, F. Galacteros & H. Wajcman. (1996) Hb Aubenas [β26(B8)GLU→GLY]: A new Variant Normally Synthesized, Affecting the Same Codon as in Hb E. Hemoglobin 20:2, pages 113-124.
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G. Nozari, S. Rahbar, A. Golshaiyzan & S. Rahmanzadeh. (1995) Molecular Analyses of β-Thalassa in Iran. Hemoglobin 19:6, pages 425-431.
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C. Wildmann, Y. Larondelle, J. L. Vaerman, R. Eeckels, P. Martiat & M. Philippel. (1993) An Initiation Codon Mutation as a Cause of β-Thalassemia in a Belgian Family. Hemoglobin 17:1, pages 19-30.
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I. E. Ogden, D. Coghlan, G. Jones, K. A. Denton, R. Harris, B. Chan, J. Woodrow & M. T. Wilson. (1992) Expression and Assembly of Functional Human Hemoglobin in S.Cerevisiae. Biomaterials, Artificial Cells and Immobilization Biotechnology 20:2-4, pages 473-475.
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S. Rahbar, G. Nozari, Y. Asmerom, P. A. Martin, C. H. Yeh & T. D. Lee. (1992) Association of HB Hope [β 136(H14)GLY→ASP] and α-THALASSEMIA-2 (3.7 KB Deletion) Causing Severe Microcytic Anemia. Hemoglobin 16:5, pages 421-425.
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Articles from other publishers (7)
Vetter, Neu‐Yilik, Kohne, Arnold, Sinha, Gaedicke, Ivančevič & A. E. Kulozik. (2001) Dominant β‐thalassaemia: a highly unstable haemoglobin is caused by a novel 6 bp deletion of the β‐globin gene. British Journal of Haematology 108:1, pages 176-181.
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