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Hemoglobin
international journal for hemoglobin research
Volume 14, 1990 - Issue 1
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Original Article

β-Thalassemia in Bulgaria

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Pages 25-33 | Received 01 Dec 1989, Accepted 18 Jan 1990, Published online: 07 Jul 2009

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Read on this site (10)

Ferda Ozkinay, Huseyin Onay, Emin Karaca, Esra Arslan, Biray Erturk, Asli Ece Solmaz, Ismihan Merve Tekin, Ozgur Cogulu, Yeşim Aydinok & Canan Vergin. (2015) Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation. Hemoglobin 39:4, pages 230-234.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Georgi H. Petkov & Georgi D. Efremov. (2007) Molecular Basis of β-Thalassemia and Other Hemoglobinopathies in Bulgaria: An Update. Hemoglobin 31:2, pages 225-232.
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Esra Birben, Cihan Öner, Reyhan Öner, Hatice Mergen, Akif Yesilipek, Fatma Gümrük, Aytemiz Gürgey & Çigdem Altay. (2001) SEVERE β THALASSEMIA IN FRAMESHIFT CODON 6 (–A) HOMOZYGOTES: EFFECTS OF HAPLOTYPE ON PHENOTYPE. Hemoglobin 25:4, pages 441-445.
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L. Stefanis, E. Kanavakis, J. Traeger-Synodinos, M. Tzetis, A. Metaxotou-Mavromati & C. Kattamis. (1994) Hematologic Phenotype of the Mutations Ivs1-n6 (T →. C), lVS1-n110 (C → A), AND CD39 (C → T) IN CARRIERS OF P-THALASSEMIA IN GREECE. Pediatric Hematology and Oncology 11:5, pages 509-517.
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M. R. Noori-Daloii, N. Moazami, S. Farhangi, A. Atalay, I. N. Geren, L. Akar, E. O. Atalay, B. Clirakoglu & E. Bermek. (1994) β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm. Hemoglobin 18:6, pages 449-453.
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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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R. Öner, S. Agarwal, A. J. Dimovski, G. D. Efremov, G. H. Petkov, C. Altay, A. Gurgey & T. H.J. Huisman. (1991) The G→A Mutation at Position +22 31 to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia. Hemoglobin 15:1-2, pages 67-76.
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Articles from other publishers (12)

Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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G Efremov. (2008) Thalassemias and Other Hemoglobinopathies in Former Yugoslavia. Balkan Journal of Medical Genetics 11:1, pages 11-26.
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A. Keenleyside & K. Panayotova. (2006) Cribra orbitalia and porotic hyperostosis in a Greek colonial population (5th to 3rd centuries BC) from the Black Sea. International Journal of Osteoarchaeology 16:5, pages 373-384.
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R. Talmaci, J. Traeger‐Synodinos, E. Kanavakis, D. Coriu, D. Colita & L. Gavrila. (2007) Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population. Journal of Cellular and Molecular Medicine 8:2, pages 232-240.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1998) 1 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 1-51.
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G.O. Tadmouri, Ş. Tüzmen, H. Özçelik, A. Özer, S.M. Baig, E.B. Senga & A.N. Başak. (1998) Molecular and population genetic analyses of β-Thalassemia in Turkey. American Journal of Hematology 57:3, pages 215-220.
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Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1993) 8 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 6:1, pages 215-262.
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G. W. Hall, R. A. Barnetson & S. L. Thein. (2008) Beta thalassaemia in the indigenous British population. British Journal of Haematology 82:3, pages 584-588.
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A. N. Başak, H. Özçelik, A. Özer, A. Tolun, M. Aksoy, L. Ağaoğlu, F. Ridolfi, L. Ulukutlu, N. Akar, A. Gürgey & B. Kirdar. (1992) The molecular basis of β-thalassemia in Turkey. Human Genetics 89:3, pages 315-318.
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A. E. Kulozik. (1992) β-thalassaemia: Molecular pathogenesis and clinical variability. European Journal of Pediatrics 151:2, pages 78-84.
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T. H. J. Huisman. (2008) FREQUENCIES OF COMMON β ‐THALASSAEMIA ALLELES AMONG DIFFERENT POPULATIONS: VARIABILITY IN CLINICAL SEVERITY . British Journal of Haematology 75:4, pages 454-457.
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