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Luhao Han, Hai Su, Hao Wu, Weiying Jiang & Suqin Chen. (2016) Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China. Hemoglobin 40:3, pages 179-186.
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Silvana F. Fonseca, Jose P. Moura Neto & Marilda S. Goncalves. (2013) Prevalence and Molecular Characterization of β-Thalassemia in the State of Bahia, Brazil: First Identification of Mutation HBB: c.135delC in Brazil. Hemoglobin 37:3, pages 285-290.
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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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Hossein Heli, Siamak Mirtorabi & Khashayar Karimian. (2011) Advances in iron chelation: an update. Expert Opinion on Therapeutic Patents 21:6, pages 819-856.
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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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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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Mohammad Ali Ehsani, Amir Abbas Hedayati-Asl, Alireza Bagheri, Syrus Zeinali & Armin Rashidi. (2009) HYDROXYUREA-INDUCED HEMATOLOGICAL RESPONSE IN TRANSFUSION-INDEPENDENT BETA-THALASSEMIA INTERMEDIA: Case Series and Review of Literature. Pediatric Hematology and Oncology 26:8, pages 560-565.
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Peyman Eshghi, Armin Rashidi, Azita Zadeh-Vakili & Ebrahim Miri-Moghadam. (2008) Hematological Phenotype of the IVS-I-5 (G > C) β-Thalassemia Mutation and Assessment of Iran's National Screening Criteria. Hemoglobin 32:5, pages 440-445.
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Articles from other publishers (6)
Ghasem Miri-Aliabad, Seyed Mohammad Nasiraldin Tabatabaei, Zahra Vaezi, Afshin Amini & Leila Asgarzadeh. (2021) Causes of Birth of More Than One Thalassemia Major Patient in Families in South-east of Iran: Lessons for Prevention Programs. Health Scope 10:3.
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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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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-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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M. L. Black, S. Sinha, S. Agarwal, R. Colah, R. Das, M. Bellgard & A. H. Bittles. (2010) A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka. Journal of Community Genetics 1:3, pages 149-157.
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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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