Citations (26)
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Niloofar Bazazzadegan, Seyedeh Sedigheh Abedini, Azita Azarkeivan, Susan Banihashemi, Nooshin Nikzat, Hossein Najmabadi & Maryam Neishabury. (2023) The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran. Hemoglobin 47:4, pages 147-151.
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Masoumeh Jalilian, Farid Azizi Jalilian, Leila Ahmadi, Razieh Amini, Hossein Esfehani, Maryam Sosanian, Bahareh Rabbani, Majid Maleki & Nejat Mahdieh. (2017) The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran. Hemoglobin 41:1, pages 61-64.
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Masomeh Mehrabi, Reza Alibakhshi, Soheila Fathollahi & Mohammad Reza Farshchi. (2013) The Spectrum of β-Thalassemia Mutations in Kermanshah Province in West Iran and its Association with Hematological Parameters. Hemoglobin 37:6, pages 544-552.
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Ebrahim Miri-Moghaddam, Azita Zadeh-Vakili, Abbas Nikravesh, Shohreh Sanei Sistani & Mehrnaz Naroie-Nejad. (2013) Sistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran. Hemoglobin 37:2, pages 138-147.
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Ebrahim Miri-Moghaddam & Azita Zadeh-Vakili. (2012) Profile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran. Hemoglobin 36:5, pages 456-463.
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Hamid Galehdari, Bahaoddin Salehi, Somaiyeh Azmoun, Bijan Keikhaei, Khoda Morad Zandian & Mohammad Pedram. (2010) Comprehensive Spectrum of the β-Thalassemia Mutations in Khuzestan, Southwest Iran. Hemoglobin 34:5, pages 461-468.
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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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Rasoul Salehi, Christopher A. Fisher, Patricia A. Bignell, Gilda Eslami & John M. Old. (2010) Identification of Three Novel Mutations [−41 (A>C), codon 24 (–G), and IVS-I-109 (−T)], in a Study of β-Thalassemia Alleles in the Isfahan Region of Iran. Hemoglobin 34:1, pages 115-120.
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Mehdi Haghi, Abbas Ali Hosseinpour Feizi, Mohammad Ali Hosseinpour Feizi, Nasser Pouladi & A. Nazli Başak. (2009) Is the Frameshift Codons 8/9 (+G) [FSC 8/9 (+G)] β-Thalassemia Mutation, Detected by the Polymerase Chain Reaction-Amplification Refractory Mutation System, Really FSC 8/9 (+G)?. Hemoglobin 33:3-4, pages 279-282.
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Mehdi Haghi, Shohre Khorshidi, Mohammad Ali Hosseinpour Feizi, Nasser Pouladi & Abbas A. Hosseinpour Feizi. (2009) β-Thalassemia Mutations in the Iranian Kurdish Population of Kurdistan and West Azerbaijan Provinces. Hemoglobin 33:2, pages 109-114.
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Mehdi Haghi, Abbas A. Hosseinpour Feizi, Cornelis L. Harteveld, Nasser Pouladi & Mohammad A. Hosseinpour Feizi. (2009) Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family. Hemoglobin 33:1, pages 75-80.
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Articles from other publishers (15)
Seyed Saeed Mousavi, Hossein Karami, Ahmad Tamadoni, Hassan Mahmoudi, Ramin Shekarriz, Rita Siami & Mohammad Bagher Hashemi-Soteh. (2024) Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran. BioMed Research International 2024, pages 1-11.
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Narmeen Ahmad, Hersh Karim, Luqman Rasool, Khanzad Ali, Mohammed Mahmood, Tara Osman & Chawan Hamakhan. (2023) A SPECTRUM OF Β-THALASSEMIA MUTATIONS IN SULAIMANI PROVINCE OF IRAQ: IDENTIFICATION OF NOVEL MUTATIONS. JOURNAL OF SULAIMANI MEDICAL COLLEGE 13:4, pages 7.
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Mehran Karimi, Tahereh Zarei, Ardeshir Bahmanimehr, Azam Aramesh, Saeed Daryanoush & Sezaneh Haghpanah. (2021) Long-term safety and efficacy of hydroxyurea in patients with non-transfusion-dependent β-thalassemia: a comprehensive single-center experience. Annals of Hematology 100:12, pages 2901-2907.
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Mohsen Anafje, Kaveh Jaseb & Homayon Yousefi. (2021) Association Between Serum Ferritin Level and Gene Mutations in Patients with Thalassemia Major and Intermediate. Jundishapur Journal of Chronic Disease Care 10:1.
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Nasir Al-Allawi, Sarah Al Allawi & Sana D. Jalal. (2020) Genetic epidemiology of hemoglobinopathies among Iraqi Kurds. Journal of Community Genetics 12:1, pages 5-14.
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Seyed Mohammad Bagher Hashemi‐Soteh, Hossein Karami, Seyed Saeid Mousavi, Touraj Farazmandfar & Ahmad Tamadoni. (2019) Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. Journal of Clinical Laboratory Analysis 34:1.
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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.
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Sharifeh Khosravi, Mansour Salehi, Mahboobeh Ramezanzadeh, Hamed Mirzaei & Rasoul Salehi. (2016) Novel Multiplex Fluorescent PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia. Archives of Medical Research 47:4, pages 293-298.
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Zohreh Rahimi. (2013) Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran. BioMed Research International 2013, pages 1-10.
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E. Miri‐Moghaddam, A. Zadeh‐Vakili, Z. Rouhani, M. Naderi, P. Eshghi & A. Khazaei Feizabad. (2011) Molecular basis and prenatal diagnosis of β‐thalassemia among Balouch population in Iran. Prenatal Diagnosis 31:8, pages 788-791.
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Haleh Akhavan-NiakiSiamak Shafiezadeh SerestiBeheshteh AsghariAli Banihashemi. (2011) IVSII-666 of Human Beta-Globin Gene: A Polymorphic Marker Linked to Codon 8(-AA) Mutation. Genetic Testing and Molecular Biomarkers 15:7-8, pages 573-576.
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Haleh Akhavan-Niaki, Poupak Derakhshandeh-Peykar, Ali Banihashemi, Amrollah Mostafazadeh, Beheshteh Asghari, Mohammad-Reza Ahmadifard, Mandana Azizi, Ali Youssefi & Maryam Mitra Elmi. (2011) A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population. Blood Cells, Molecules, and Diseases 47:1, pages 29-32.
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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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Owen T. M. Chan, Kenneth D. Westover, Lisa Dietz, James L. Zehnder & Iris Schrijver. (2010)
Comprehensive and Efficient
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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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