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Hemoglobin
international journal for hemoglobin research
Volume 35, 2011 - Issue 4
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Original Article

The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters

Seyedeh Fatemeh MoosaviMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran
,
Azam AmirianMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran
,
Behnaz ZarbakhshMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran
,
Alireza KordafshariMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran
,
Hasan MirzahoseiniMedical Biotechnology Department, Biotechnology Research Center, Pasteur Institute of Iran
,
Sirous ZeinaliMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran
&
Morteza KarimipoorMolecular Medicine Department, Biotechnology Research Center, Pasteur Institute of IranCorrespondence[email protected]
 show all
Pages 323-330 | Received 12 Jan 2011, Accepted 12 Feb 2011, Published online: 28 Jul 2011

Citations (14)

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Seyedeh Sedigheh Abedini, Fatemeh Forouzesh Pour, Keyvan Karimi, Zhila Ghaderi, Samaneh Farashi, Ameneh Tavakoli Koudehi, Homeira Javadi Pirouz, Seyedeh Bahareh Mobini Nejad, Azita Azarkeivan & Hossein Najmabadi. (2018) Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian Population. Hemoglobin 42:4, pages 252-256.
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Hossein Jalali, Mohammad Reza Mahdavi, Payam Roshan, Mehrnoush Kosaryan, Hosein Karami & Mehrad Mahdavi. (2014) Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012. Hematology 19:4, pages 192-195.
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Articles from other publishers (12)

Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati & Marziye Mohammadi‐Anaei. (2021) Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual. eJHaem 2:3, pages 366-374.
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Stacy Colaco & Anita Nadkarni. (2021) Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation Research/Reviews in Mutation Research 788, pages 108387.
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Hailong Huang, Liangpu Xu, Meihuan Chen, Na Lin, Huili Xue, Lingji Chen, Yan Wang, Deqin He, Min Zhang & Yuan Lin. (2019) Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China. Scientific Reports 9:1.
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Sheng He, Jihui Li, Dong Ming Li, Shang Yi, Xiongcai Lu, Yudi Luo, Yi Liang, Chunfeng Feng, Biyan Chen, Chenguang Zheng & Xiaoxia Qiu. (2018) Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China. Gene 655, pages 61-64.
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Sheng He, Qian Qin, Shang Yi, Yuan Wei, Li Lin, Shaoke Chen, Jianping Deng, Xianmin Xu, Chenguang Zheng & Biyan Chen. (2017) Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China. Gene 619, pages 71-75.
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Hossein Jalali, Mehrnoush Kosaryan, Mohammad Reza Mahdavi & Mehrad Mahdavi. (2017) Co-inheritance of --MED double gene deletion and αααAnti3.7 triplication on α-globin gene in Mazandaran at 2016. Research in Molecular Medicine 5:1, pages 44-47.
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Lingling Hu, Xuan Shang, Sheng Yi, Ren Cai, Zhetao Li, Cuixian Liu, Yidan Liang, Decheng Cai, Feng Zhang & Xiangmin Xu. (2016) Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families. Molecular Genetics and Genomics 291:3, pages 1443-1450.
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Sevcan Tug Bozdogan, Ozge Ozalp Yuregir, Nurhilal Buyukkurt, Huseyin Aslan, Zeynep Canan Ozdemir & Tomasz Gambin. (2014) Alpha-Thalassemia Mutations in Adana Province, Southern Turkey: Genotype-Phenotype Correlation. Indian Journal of Hematology and Blood Transfusion 31:2, pages 223-228.
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Majid Naderi, Ibrahim Miri-Moghaddam, Akbar Dorgalaleh, Shaban Alizadeh, Shadi Tabibian & Masoud Pishjoo. (2015) A Patient With Coinheritance of Alpha-Globin Gene Triplication and IVSI-5 Mutation of Beta-Globin Gene. Zahedan Journal of Research in Medical Sciences 17:5.
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Xiu-Yun Yao, Jie Yu, Shi-Ping Chen, Jian-Wen Xiao, Qi-Chen Zheng, Hai-Yan Liu, Lei Zhang, Ying Xian & Lin Zou. (2013) Prevalence and genetic analysis of α-thalassemia and β-thalassemia in Chongqing area of China. Gene 532:1, pages 127-131.
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Muhammet Murat Celik, Ramazan Gunesacar, Gonul Oktay, Gulay Gulbol Duran & Hasan Kaya. (2013) Spectrum of α-thalassemia mutations including first observation of - -FIL deletion in Hatay Province, Turkey. Blood Cells, Molecules, and Diseases 51:1, pages 27-30.
Crossref
Wan-Jun Zhou, Wei-Yu Liu, Dun Liu, Jian-Hui Jiang, Dian-Min Zhou, Ze-Yan Zhong & Xiang-Min Xu. (2012) A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction. Analytical Biochemistry 427:2, pages 144-150.
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