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Hemoglobin
international journal for hemoglobin research
Volume 17, 1993 - Issue 5
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Original Article

The β- and δ-Thalassemia Repository (Seventh Edition)

Pages 479-499 | Published online: 07 Jul 2009

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (9)

Ghazi O. Tadmouri & A. Nazlı Başak. (2001) β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTS. Hemoglobin 25:2, pages 227-239.
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M. A. Çürük, S. C. Howard, A. Kutlar & T. H. J. Huisman. (1995) A Newly Discovered β°-Thalassemia (IVS-11-850, G→A) Mutation in a North European Family. Hemoglobin 19:3-4, pages 207-211.
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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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M. A.F. El-Hazmi, A. S. Warsy & A. R. Al-Swailem. (1995) The Frequency of 14 β-Thalassemia Mutations in the Arab Populations. Hemoglobin 19:6, pages 353-360.
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L. Pagano, S. Desicato, A. Viola, C. De Rosa & G. Fioretti. (1995) Identification of the -92 (C→T) Mutation by the Amplification Refractory Mutation Sym in Southern Italy. Hemoglobin 19:5, pages 307-310.
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P. L. Pande, S. Prakash, R. S. Tiwary, E. G. Kazanetz, J. Ye. Leonova & T. H.J. Huisman. (1995) β-Thalassemia Intermedia in An Indian Female h the Hb Hofu [β126(H4)Val→Glu]-(β°-Thalassemia [Codons 8/9 (+G)] Combination. Hemoglobin 19:5, pages 301-306.
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L. Jankovic, D. Plaseska, G. D. Efremov, P. Tchaicarova & G. H. Petkov. (1994) Two Rare Mutations [CD 30 (G->C) and CDs 36/37 (−T)] in a Turkish Thalassemia Major Patient from Bulgaria. Hemoglobin 18:4-5, pages 359-364.
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M. F. G. Sadiq & T. H. J. Huisman. (1994) Molecular Characterization of β-Thalassemia in North Jordan. Hemoglobin 18:4-5, pages 325-332.
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Articles from other publishers (15)

D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Ariel Roldán, Marina Gutiérrez, Ana Cygler, Mariana Bonduel, Gabriela Sciuccati & Aurora Feliu Torres. (1997) Molecular characterization of β-thalassemia genes in an Argentine population. American Journal of Hematology 54:3, pages 179-182.
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A. Colosimo, G. Novelli, A. Cavicchini & B. Dallapiccola. (1996) Detection of eight β-thalassemia mutations using a DNA enzyme immunoassay. International Journal of Clinical & Laboratory Research 26:2, pages 136-139.
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Catherine Badens, Isabelle Thuret, Gérard Michel, Mickaël Krawczak, Jean-François Mattei, Danielle Lena-Russo, Dominique Labie & Jacques Elion. (1996) Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the β-globin gene. Human Mutation 8:1, pages 89-92.
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Deborah Rund & Eliezer Rachmilewitz. (1995) Advances in the pathophysiology and treatment of thalassemia. Critical Reviews in Oncology/Hematology 20:3, pages 237-254.
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G. R. Gray, H. E. Manson, L‐H. Gu, J. Ye. Leonova & T. H. J. Huisman. (2006) Hb lulu island (α 2 β 2 107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia . American Journal of Hematology 50:1, pages 26-29.
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XIANGMIN Xu, CAN LIAO, ZHONGYING LIU, JIAN LI, ZHAOHUI PENG, LUO‐LIN QIU & JIZENG ZHANG. (2008) A novel amber mutation in a β°‐thalassaemia gene (β 37 TGG→TAG), with direct detection by mapping the restriction fragments in amplified genomic DNA . British Journal of Haematology 90:4, pages 960-962.
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PRANEE SUTCHARITCHAN, RANDALL SAIKI, SUTHAT FUCHAROEN, PRANEE WINICHAGOON, HENRY ERLICH & STEPHEN H. EMBURY. (2008) Reverse dot‐blot detection of Thai β‐thalassaemia mutations. British Journal of Haematology 90:4, pages 809-816.
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Britta Landin, Olle Rudolphi & BÖRje Ek. (2006) Initiation codon mutation (ATG → ATA) of the β‐globin gene causing β‐thalassemia in a Swedish family. American Journal of Hematology 48:3, pages 158-162.
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T. H. J. Huisman. 1995. Hereditary Diseases and Blood Transfusion. Hereditary Diseases and Blood Transfusion 53 61 .
Dvora Filon, Varda Oron, Ragda Shawa, Elham Elborno, Khamis Najjar, Theodore Tulchinsky, Eliezer Rachmilewitz, Deborah Rund & Ariella Oppenheim. (1995) Spectrum of β-thalassemia mutations in the Gaza area. Human Mutation 5:4, pages 351-353.
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G. Schilirò, F. di Gregorio, P. Samperi, E. Mirabile, R. Liang, M. A. Cürük, Z. Ye & T. H. J. Huisman. (2006) Genetic heterogeneity of β‐thalassemia in southeast sicily. American Journal of Hematology 48:1, pages 5-11.
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Shu-zhen Huang, Fan-yi Zeng, Zhao-rui Ren, Zhi-hong Lu, Griffin P. Rodgers, Alan N. Schechter & Yi-tao Zeng. (1994) RNA transcripts of the β-thalassaemia allele IVS-2–654 C → T: a small amount of normally processed β-globin mRNA is still produced from the mutant gene. British Journal of Haematology 88:3, pages 541-546.
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E. Baysal & T. H. J. Huisman. (2006) Detection of common deletional α‐thalassemia‐2 determinants by PCR. American Journal of Hematology 46:3, pages 208-213.
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R. Liang, S. Liang, N. H. Jiang, X‐J. Wen, J‐B. Zhao, J. F. Nechtman, T. A. Stoming & T. H. J. Huisman. (2008) α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization. British Journal of Haematology 86:2, pages 351-354.
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