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

Molecular Characterization of β-Thalassehia in the United Arab Emirates

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Pages 355-362 | Received 27 Oct 1992, Accepted 27 Apr 1993, Published online: 07 Jul 2009

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Read on this site (8)

Srdjan Denic, Bashir Aden, Nico Nagelkerke & Awad Al Essa. (2013) β-Thalassemia in Abu Dhabi: Consanguinity and Tribal Stratification are Major Factors Explaining the High Prevalence of the Disease. Hemoglobin 37:4, pages 351-358.
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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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S. El-Kalla & A. R. Mathews. (1997) HB D-Punjab in the United Arab Emirates. Hemoglobin 21:4, pages 369-375.
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S. El-Kalla & A. R. Mathews. (1997) A Novel β-Thalassemia Mutation [Codon 45 (-T)] in a Pakistani Family. Hemoglobin 21:6, pages 499-503.
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S. El-Kalla & A. R. Mathews. (1997) A Significant β-Thalassemia Heterogeneity in the United Arab Emirates. Hemoglobin 21:3, pages 237-247.
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S. El-kalla & A. R. Mathews. (1995) A Novel Frameshift Mutation Causing β-Thalassemia in a Sikh. Hemoglobin 19:3-4, pages 183-189.
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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 (9)

Srdjan Denic, Mukesh M. Agarwal, Bayan Al Dabbagh, Awad El Essa, Mohamed Takala, Saad Showqi & Javed Yassin. (2013) Hemoglobin A 2 Lowered by Iron Deficiency and α -Thalassemia: Should Screening Recommendation for β -Thalassemia Change? . ISRN Hematology 2013, pages 1-5.
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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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Yousef M. Abdulrazzaq, Ahmed Ibrahim, Abdulla I. Al-Khayat & Kenneth Dawson. (2005) β-Thalassemia major and its effect on amino acid metabolism and growth in patients in the United Arab Emirates. Clinica Chimica Acta 352:1-2, pages 183-190.
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N. J. Makhoul, R. S. Wells, H. Kaspar, H. Shbaklo, A. Taher, N. Chakar & P. A. Zalloua. (2005) Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration. Annals of Human Genetics 69:1, pages 55-66.
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M.F. Sadiq, A. Eigel & J. Horst. (2001) Spectrum of β‐thalassemia in Jordan: Identification of two novel mutations. American Journal of Hematology 68:1, pages 16-22.
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Soren Blau. (2001) Limited yet informative: pathological alterations observed on human skeletal remains from third and second millennia bc collective burials in the United Arab Emirates. International Journal of Osteoarchaeology 11:3, pages 173-205.
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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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R. De Leo, G. Deidda, A. Novelletto, S. El-Kalla, A. R. Mathews & L. Felicetti. (1995) Analysis of β-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSINT 5 (G-C) mutation. Human Mutation 5:4, pages 327-328.
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