Citations (32)
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Ahmad Shoujaa, Faten Moasses, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2020) Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study. Hemoglobin 44:1, pages 42-46.
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Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2019) Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report. Hemoglobin 43:4-5, pages 283-285.
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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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Hussam Ghoti, Eitan Fibach, Eliezer A. Rachmilewitz, Hisham Jeadi & Dvora Filon. (2017) New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F. Hemoglobin 41:2, pages 144-146.
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Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty & Walid Al-Achkar. (2014) Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population. Hemoglobin 38:6, pages 390-393.
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Ozgur Aldemir, Muzeyyen Izmirli & Hasan Kaya. (2014) The Spectrum of β-Thalassemia Mutations in Hatay, Turkey: Reporting Three New Mutations. Hemoglobin 38:5, pages 325-328.
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Rami A. Jarjour, Hossam Murad, Faten Moasses & Walid Al-Achkar. (2014) Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations. Hemoglobin 38:4, pages 272-276.
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Nasir A.S. Al-Allawi, Bassam M.S. Al-Mousawi, Ameer I.A. Badi & Sana D. Jalal. (2013) The Spectrum of β-Thalassemia Mutations in Baghdad, Central Iraq. Hemoglobin 37:5, pages 444-453.
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Nasir A.S. Al-Allawi, Sana D. Jalal, Farida F. Nerwey, Galawezh O.O. Al-Sayan, Sahima S.M. Al-Zebari, Awny A. Alshingaly, Raji D. Markous, Jaladet M.S. Jubrael & Hanan Hamamy. (2012) Sickle Cell Disease in the Kurdish Population of Northern Iraq. Hemoglobin 36:4, pages 333-342.
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Essam H. Jiffri, Neda Bogari, Khaled H. Zidan, Salwa Teama & Nasser A. Elhawary. (2010) Molecular Updating of β-Thalassemia Mutations in the Upper Egyptian Population. Hemoglobin 34:6, pages 538-547.
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Sana D. Jalal, Nasir A.S. Al-Allawi, Nooshin Bayat, Hasham Imanian, Hossein Najmabadi & Azad Faraj. (2010) β-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq. Hemoglobin 34:5, pages 469-476.
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Othman E. Soliman, Sohier Yahia, Amany Shouma, Hala K. Shafiek, Ashraf E. Fouda, Hanan Azzam, Nashwa K. Abousamra, Rabab Mahfouz, Enas F. Goda & Solafa A. El-Sharawy. (2010) Reverse hybridization StripAssay detection of β-thalassemia mutations in northeast Egypt. Hematology 15:3, pages 182-186.
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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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Nasir A.S. Al-Allawi, Jalaldet M.S. Jubrael & Michael Hughson. (2006) Molecular Characterization of β-Thalassemia in the Dohuk Region of Iraq. Hemoglobin 30:4, pages 479-486.
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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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Mahmoud Abd El-Latif, Dvora Filon, Deborah Rund, Ariella Oppenheim & Moien Kanaan. (2002) THE β+-IVS-I-6 (T → C) MUTATION ACCOUNTS FOR HALF OF THE THALASSEMIA CHROMOSOMES IN THE PALESTINIAN POPULATIONS OF THE MOUNTAIN REGIONS. Hemoglobin 26:1, pages 33-40.
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Antroulla Kyrri, Xenia Felekis, Eleni Kalogerou, George Christopoulos, Christiana Makariou, Dena Loizidou & Marina Kleanthous. (2001) Hb LIMASSOL [β8(A5)Lys → Asn]: A NEW HEMOGLOBIN VARIANT. Hemoglobin 25:4, pages 421-424.
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John M. Old, Shaheen N. Khan, Ishwar Verma, Suthat Fucharoen, Marina Kleanthous, Panos Ioannou, Navaratnam Kotea, Christopher Fisher, Sheikh Riazuddin, Renu Saxena, Pranee Winichagoon, Kyriacos Kyriacou, Faizeh Al-Quobaili & Baldip Khan. (2001) A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION. Hemoglobin 25:4, pages 397-407.
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Articles from other publishers (14)
Roula ShakkourTaghrid HammoudYasser MukhalalatyFaizeh Al Quobaili. (2021) Investigation of Gonadal Function, Puberty, and their relationship to Serum Ferritin in Male patients with β-Thalassemia major in Syria. Research Journal of Pharmacy and Technology, pages 3595-3602.
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Ahmet Kursad Gunes & Hilmi Erdem Gozden. (2021) The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens. Cureus.
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Hatice Çevirici, Can Acıpayam, Ebru Dündar Yenilmez, Fatma Burcu Belen, Esra Pekpak, Yöntem Yaman & Abdullah Tuli. (2019) Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major. Turkish Journal of Biochemistry 44:2, pages 126-129.
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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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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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G. Christopoulos, G.M. Ezzat & M. Kleanthous. (2012) Use of denaturing gradient gel electrophoresis in screening unknown β-thalassemia mutations in Egyptian patients. Egyptian Journal of Medical Human Genetics 13:3, pages 343-349.
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Nasir A. S. Al-Allawi, Kawa M. A. Hassan, Anwar K. Sheikha, Farida F. Nerweiy, Raji S. Dawood & Jaladet Jubrael. (2010) -Thalassemia Mutations among Transfusion-Dependent Thalassemia Major Patients in Northern Iraq. Molecular Biology International 2010, pages 1-4.
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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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Nicos Skordis, Monica Michaelidou, Savvas C. Savva, Yiannis Ioannou, Andreas Rousounides, Marina Kleanthous, George Skordos & Soteroulla Christou. (2006) The impact of genotype on endocrine complications in thalassaemia major. European Journal of Haematology 77:2, pages 150-156.
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Amel Haj Khelil, Sandrine Laradi, Abdelhedi Miled, Ghazi Omar Tadmouri, Jemni Ben Chibani & Pascale Perrin. (2004) Clinical and molecular aspects of haemoglobinopathies in Tunisia. Clinica Chimica Acta 340:1-2, pages 127-137.
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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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