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Hemoglobin
international journal for hemoglobin research
Volume 17, 1993 - Issue 4
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Miscellaneous Article

A Novel Deletion in a Turkish β-Thalassewia Patient Detected by DGGE and Direct Sequencing: FSC 22–24 (-7 bp)

H. Özçelik Bogaziçi University, Department of Biology, Istanbul, Turkey
,
A. N. Başak Bogaziçi University, Department of Biology, Istanbul, Turkey
,
Ş. Tüzmen Bogaziçi University, Department of Biology, Istanbul, Turkey
,
B. Kirdar Bogaziçi University, Department of Biology, Istanbul, Turkey
&
N. Akar Ankara University, School of Medicine Children's Hospital, Ankara, Turkey
Pages 387-391 | Received 19 Oct 1992, Accepted 25 Mar 1993, Published online: 07 Jul 2009

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Anita Nadkarni, Ajit Gorakshakar, Reema Surve, Pratibha Sawant, Supriya Phanasgaonkar, Sona Nair, Kanjaksha Ghosh & Roshan B. Colah. (2009) Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population. Hemoglobin 33:1, pages 59-65.
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Ramachandran V. Shaji, Nathalie Gerard, Rajagopal Krishnamoorthy, Alok Srivastava & Mammen Chandy. (2002) A NOVEL β-THALASSEMIA MUTATION IN AN ASIAN INDIAN. Hemoglobin 26:1, pages 49-57.
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Ibrahim Keser, Ozlem G. Kayisli, Akif Yesilipek, Osman N. Ozes & Guven Luleci. (2001) Hb ANTALYA [CODONS 3–5 (Leu-Thr-Pro → Ser-Asp-Ser)]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA AND HIGH Hb A2. Hemoglobin 25:4, pages 369-373.
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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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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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Gülay Özcengiz. (1996) Biotechnological Developments in Turkey. Critical Reviews in Biotechnology 16:1, pages 53-94.
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E. Baysal & M. F. H. Carver. (1995) The β- and δ-Thalassemia Repository (Eighth Edition). Hemoglobin 19:3-4, pages 213-236.
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Articles from other publishers (6)

T. Bilgen, O. A. Clark, Z. Ozturk, M. Akif Yesilipek & I. Keser. (2012) Two novel mutations in the 3′ untranslated region of the beta‐globin gene that are associated with the mild phenotype of beta thalassemia. International Journal of Laboratory Hematology 35:1, pages 26-30.
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Dong-Zhi Li, Can Liao, Jian Li & Ru Li. (2009) A novel β-globin gene deletion (codons 89–93) in a Chinese family. Annals of Hematology 89:3, pages 323-325.
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Marcos A. C. Bezerra, Dulcinéia M. Albuquerque, Magnun N. N. Santos, Elza M. Kimura, Susan E. D. C. Jorge, Denise M. Oliveira, Betânia L. T. B. Domingues, Jaqueline C. Peres, Aderson S. Araújo, Fernando F. Costa & Maria F. Sonati. (2009) Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [ β 122 (GH5) Phe→Ser], a probable case of germ line mutation, and Hb Olinda [ β 22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequence . European Journal of Haematology 83:4, pages 378-382.
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ES Edison, RV Shaji, SG Devi, A Moses, A Viswabandhya, V Mathews, B George, A Srivastava & M Chandy. (2008) Analysis of β globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clinical Genetics 73:4, pages 331-337.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
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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