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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 1
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Original

THE β+-IVS-I-6 (T → C) MUTATION ACCOUNTS FOR HALF OF THE THALASSEMIA CHROMOSOMES IN THE PALESTINIAN POPULATIONS OF THE MOUNTAIN REGIONS

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Pages 33-40 | Received 27 Apr 2001, Accepted 13 Aug 2001, Published online: 07 Jul 2009

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Read on this site (14)

Shaima Al-Zebari, Nasir AS Al-Allawi & Farida Nerweyi. (2023) Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq. Hemoglobin 47:3, pages 111-117.
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Aisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, Mohamed Yassin & Hatem Zayed. (2021) The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. Expert Review of Hematology 14:1, pages 109-122.
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Leen Samha, Mahmoud M. Sirdah, N. Scott Reading, Bashar Karmi & Archana M. Agarwal. (2020) Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine. Hemoglobin 44:2, pages 128-130.
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Haiyan Luo, Yongyi Zou & Yanqiu Liu. (2020) A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family. Hemoglobin 44:1, pages 55-57.
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Hossam Murad, Faten Moassas, Ifad Ghoury & Yasser Mukhalalaty. (2018) Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients. Hemoglobin 42:5-6, pages 302-305.
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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Laudy Cherry, Carla Calo, Rodica Talmaci, Pascale Perrin & Lucian Gavrila. (2016) β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area. Hemoglobin 40:2, pages 85-96.
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Biyan Chen, Peng Huang, Shang Yi, Qiuli Chen, Yanqing Tang, Qiang Zhang & Sheng He. (2015) First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family. Hemoglobin 39:3, pages 207-208.
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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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Fekri Samarah, Suhail Ayesh, Miranda Athanasiou, John Christakis & Norma Vavatsi. (2009) βS-Globin Gene Cluster Haplotypes in the West Bank of Palestine. Hemoglobin 33:2, pages 143-149.
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Ali Asghar Kiani, Yousef Mortazavi, Sirous Zeinali & Yaghob Shirkhani. (2007) The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran. Hemoglobin 31:3, pages 343-349.
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Imen Chouk, Béchir Ben Daoud, Fethi Mellouli, Mohamed Bejaoui, Nathalie Gérard, Koussay Dellagi & Salem Abbes. (2004) Contribution to the Description of the β‐Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity. Hemoglobin 28:3, pages 189-195.
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Articles from other publishers (11)

Rashail Faraon, Mahmoud Daraghmah, Fekri Samarah & Mahmoud A. Srour. (2019) Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine. BMC Hematology 19:1.
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Anthony O. Akinbami, Amy E. Sobota, Hong-Yuan Luo, David H.K. Chui & Martin H. Steinberg. (2018) A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy. Journal of Pediatric Hematology/Oncology 40:3, pages e145-e147.
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Nikolaos Sousos, Despoina Adamidou, Philippos Klonizakis, Alexandra Agapidou, Stamatia Theodoridou, Georgios Spanos, Kyriakos Psarras, Evaggelia Vetsiou, Timoleon-Achilleas Vyzantiadis & Efthymia Vlachaki. (2017) Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence. Acta Haematologica 137:3, pages 175-182.
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Adil A. Eissa, Muna A. Kashmoola, Sulav D. Atroshi & Nasir A. S. Al-Allawi. (2014) Molecular Characterization of β-Thalassemia in Nineveh Province Illustrates the Relative Heterogeneity of Mutation Distributions in Northern Iraq. Indian Journal of Hematology and Blood Transfusion 31:2, pages 213-217.
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Ammar D. Elmezayen, Samia M. Kotb, Nadia A. Sadek & Ebtesam M. Abdalla. (2015) β-Globin Mutations in Egyptian Patients With β-Thalassemia. Laboratory Medicine 46:1, pages 8-13.
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Giulia Breveglieri, Irene Mancini, Nicoletta Bianchi, Ilaria Lampronti, Francesca Salvatori, Enrica Fabbri, Cristina Zuccato, Lucia C. Cosenza, Giulia Montagner, Monica Borgatti, Fiorella Altruda, Sharmila Fagoonee, Gianni Carandina, Michele Rubini, Vincenzo Aiello, Laura Breda, Stefano Rivella, Roberto Gambari & Alessia Finotti. (2015) Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation . BioMed Research International 2015, pages 1-20.
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Mahmoud M. Sirdah, Jürgen Sievertsen, Mansour S. Al-Yazji, Issa S. Tarazi, Ramy M. Al-Haddad, Rolf D. Horstmann & Christian Timmann. (2013) The spectrum of β-thalassemia mutations in Gaza Strip, Palestine. Blood Cells, Molecules, and Diseases 50:4, pages 247-251.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili & Massoud Houshmand. (2012) Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration. The Scientific World Journal 2012, pages 1-7.
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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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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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