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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 3
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Original Article

A Significant β-Thalassemia Heterogeneity in the United Arab Emirates

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Pages 237-247 | Received 19 Jul 1996, Accepted 06 Feb 1997, Published online: 07 Jul 2009

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Päivikki Kangastupa, Kari Åkerman, Sari Risku, Matti Väisänen, Rutta Kuusela, Jarkko Romppanen, Annika Kouki, Mia Sneck, Outi Itkonen & Onni Niemelä. (2023) The prevalence of hemoglobin Tacoma in Finland detected by HbA1c capillary electrophoresis. Scandinavian Journal of Clinical and Laboratory Investigation 83:1, pages 51-57.
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Jordyn A. Moore, Beverley M. Pullon, Darrell Wang & Stephen O. Brennan. (2021) Hb Tacoma: G>T or G>C, and Does It Matter?. Hemoglobin 45:3, pages 203-206.
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Hayley Merkeley, Nicholas Sandercock, Linda Halchuk, Manoela Braga & Madeleine Verhovsek. (2021) A novel means of identifying hemoglobin Tacoma utilizing capillary electrophoresis with a hemoglobin A1c software platform. Cogent Medicine 8:1.
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Stacy Colaco, Amee Trivedi, Roshan B. Colah, K. Ghosh & Anita H. Nadkarni. (2014) Masking of a β-Thalassemia Determinant by a Novel δ-Globin Gene Defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis. Hemoglobin 38:1, pages 24-27.
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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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Suha M. Hassan, Nishat Hamza, Fatma Jaffer Al-Lawatiya, Ali Jaffer Mohammed, Cornelis L. Harteveld, Anna Rajab & Piero C. Giordano. (2010) Extended Molecular Spectrum of β- and α-Thalassemia in Oman. Hemoglobin 34:2, pages 127-134.
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Amina Bibi, Taieb Messaoud & Slaheddine Fattoum. (2006) Haplotypes Linked to Three Rare β-Thalassemia Mutations, Originally Reported in Tunisia. Hemoglobin 30:2, pages 175-181.
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Philippe Lacan, Bénédicte Ponceau, Martine Aubry & Alain Francina. (2003) Mild Hb S-β+-Thalassemia with a Deletion of Five Nucleotides at the Polyadenylation Site of the β-Globin Gene. Hemoglobin 27:4, pages 257-260.
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K. Kyriacou, F. Al Quobaili, E. Pavlou, G. Christopoulos, P. Ioannou & M. Kleanthous. (2000) Molecular Characterization of β-Thalassemia in Syria. Hemoglobin 24:1, pages 1-13.
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B. Landin, G. Alvelius, D. K. Rai & G. Elinder. (2000) Compound Heterozygosity for Hb Tacoma [β30(B12)Arg→Ser] and β+-Thalassemia. Hemoglobin 24:3, pages 253-257.
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Salah El-Kalla & Erol Baysal. (1998) Genotype-Phenotype Correlation of Sickle Cell Disease in the United Arab Emirates. Pediatric Hematology and Oncology 15:3, pages 237-242.
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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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H. Furuumi, N. Firdous, T. Inoue, H. Ohta, P. Winichagoon, S. Fucharoen & Y. Fukumaki. (1998) Molecular Basis of β-Thalassemia in the Maldives. Hemoglobin 22:2, pages 141-151.
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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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Articles from other publishers (10)

M. E. Lokhmatova, N. E. Sokolova, M. V. Krasilnikova, E. A. Litvin, N. A. Karamjan, S. G. Mann, S. A. Plyasunova & N. S. Smetanina. (2022) Unstable abnormal hemoglobins found in Russia in the past 10 years. Pediatric Hematology/Oncology and Immunopathology 21:3, pages 13-21.
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Alexander W. Macharia, George Mochamah, Sophie Uyoga, Carolyne M. Ndila, Gideon Nyutu, Metrine Tendwa, Emily Nyatichi, Johnstone Makale, Russell E. Ware & Thomas N. Williams. (2020) β‐Thalassemia pathogenic variants in a cohort of children from the East African coast. Molecular Genetics & Genomic Medicine 8:7.
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Jamie Nourse, Stefano Spada & Sven Danckwardt. (2020) Emerging Roles of RNA 3′-end Cleavage and Polyadenylation in Pathogenesis, Diagnosis and Therapy of Human Disorders. Biomolecules 10:6, pages 915.
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Wenguang Jia, Weidong  Wang, Hengying  Zhu & Ping Chen. (2019) A Novel Mutation at HBB: c.91delA (Codon 30, –A) Causing β-Thalassemia in a Chinese Family. Acta Haematologica 142:4, pages 249-252.
Crossref
Nejat Mahdieh & Bahareh Rabbani. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews 30:6, pages 493-508.
Crossref
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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Zohreh Rahimi, Adriana Muniz & Abbas Parsian. (2009) Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Molecular Biology Reports 37:1, pages 149-154.
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Isabelle Tchou, Myriam Diepold, Pierre-Antonio Pilotto, Dorine Swinkels, Marguerite Neerman-Arbez & Photis Beris. (2009) Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia. European Journal of Haematology 83:6, pages 595-602.
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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.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .

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