Citations (15)
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Milad Rafat, Zeinab Allamehzadeh, Mohammad Shekari, Masoumeh Afsa & Kianoosh Malekzadeh. (2021) The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study. Hemoglobin 45:4, pages 234-238.
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Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali. (2020) α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. Hemoglobin 44:1, pages 20-26.
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Zahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, Mitra Yadollahi & Nariman Khosravi-Farsani. (2020) Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran. Hemoglobin 44:1, pages 27-30.
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Ebrahim Miri-Moghaddam, Sara Bahrami, Majid Naderi, Ali Bazi & Morteza Karimipoor. (2016) Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran. Hemoglobin 40:3, pages 173-178.
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Rawand P. Shamoon, Nasir A. S. Al-Allawi, Maria D. Cappellini, Elena Di Pierro, Valentina Brancaleoni & Francesca Granata. (2015) Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan. Hemoglobin 39:3, pages 178-183.
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Nabeel J. Al Moamen, Fawzia Mahdi, Ebtihal Salman, Thabet Ahmed, Ruqaya Abbas, Shaikha Al Arrayed, Hassan Sanad & Al Alawi Ahmed. (2013) Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain. Hemoglobin 37:4, pages 369-377.
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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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Mohammad Hamid, Frouzandeh Mahjoubi, Mohammad T. Akbari, Aida Arab, Sirous Zeinali & Morteza Karimipoor. (2009) Molecular Analysis of γ-Globin Promoters, HS-111 and 3′HS1, in β-thalassemia Intermedia Patients Associated with High Levels of Hb F. Hemoglobin 33:6, pages 428-438.
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Articles from other publishers (7)
Anousheh Shasttiri, Misagh Moridi, Abbas Safari, Sayed Haidar Abbas Raza, Mostafa Ghaderi-Zefrehei, Massoud Houshmand, Ahmad Oryan, Mohammad Hossein Sanati, Jacqueline Smith & Motahareh Amjadi. (2021) Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population Analysis. Biochemical Genetics 60:3, pages 987-1006.
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Mehran Modares Sadeghi, Laleh Shariati, Zahra Hejazi, Mansoureh Shahbazi, Mohammad Amin Tabatabaiefar & Hossein Khanahmad. (2017)
Inducing indel mutation in the
SOX6
gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia
. Journal of Cellular Biochemistry 119:3, pages 2512-2519.
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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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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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Shoaib Al Zadjali, Yasser Wali, Fatma Al Lawatiya, David Gravell, Salam AlKindi, Kareema Al Falahi, Rajagopal Krishnamoorthy & Shahina Daar. (2011) The β-globin promoter −71 C>T mutation is a β+ thalassemic allele. European Journal of Haematology 87:5, pages 457-460.
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Aida Arab, Morteza Karimipoor, Ali Rajabi, Mohammad Hamid, Sedeigheh Arjmandi & Sirous Zeinali. (2010) Molecular characterization of β-thalassemia intermedia: a report from Iran. Molecular Biology Reports 38:7, pages 4321-4326.
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Maryam Neishabury, Azita Azarkeivan & Hossein Najmabadi. (2010) Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation. Blood Cells, Molecules, and Diseases 44:2, pages 95-99.
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