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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 1
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High Prevalence of the −α3.7 Deletion Among Thalassemia Patients in Iran

Maryam Neishabury Genetics Research Center, The Social Welfare and Rehabilitation Sciences University, Daneshjoo Boulevard, Koodakyar Avenue, Evin, Tehran, 19834, Iran
,
Christian Oberkanins ViennaLab Labordiagnostika GmbH, Vienna, Austria
,
Lia Abbasi Moheb Genetics Research Center, The Social Welfare and Rehabilitation Sciences University, Daneshjoo Boulevard, Koodakyar Avenue, Evin, Tehran, 19834, Iran
,
Ali Akbar Pourfathollah Tarbiat Modarres University, School of Medical Sciences, Tehran, Iran
,
Kimia Kahrizi Genetics Research Center, The Social Welfare and Rehabilitation Sciences University, Daneshjoo Boulevard, Koodakyar Avenue, Evin, Tehran, 19834, Iran
,
Elahe Keyhany Genetics Research Center, The Social Welfare and Rehabilitation Sciences University, Daneshjoo Boulevard, Koodakyar Avenue, Evin, Tehran, 19834, Iran
,
Walter Krugluger Institute of Clinical Chemistry, Rudolfstiftung Hospital, Vienna, Austria
&
Hossein Najmabadi Genetics Research Center, The Social Welfare and Rehabilitation Sciences University, Daneshjoo Boulevard, Koodakyar Avenue, Evin, Tehran, 19834, Iran
 show all
Pages 53-55 | Received 02 Feb 2002, Accepted 01 Oct 2002, Published online: 07 Jul 2009

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Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Fatemeh Forouzesh Pour, Fatemeh Zeinali, Fariba Rad, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2016) Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene. Hemoglobin 40:1, pages 38-43.
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Samaneh Farashi, Shadi Vakili, Negin F. Garous, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia. Hemoglobin 39:6, pages 398-402.
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Samaneh Farashi, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes. Expert Review of Hematology 8:5, pages 693-698.
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Javad Dehbozorgian, Mohamad Moghadam, Saeed Daryanoush, Sezaneh Haghpanah, Jaber Imani fard, Azam Aramesh, Amin Shahsavani & Mehran Karimi. (2015) Distribution of alpha-thalassemia mutations in Iranian population. Hematology 20:6, pages 359-362.
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Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi. (2014) Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin 38:3, pages 153-157.
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Nooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, Negin Faramarzi, Mehri Ashki, Shadi Vakili, Hashem Imanian, Mohsen Khosravi, Azita Azar-Keivan & Hossein Najmabadi. (2013) Novel Mutations Responsible for α-Thalassemia in Iranian Families. Hemoglobin 37:2, pages 148-159.
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Seyedeh Fatemeh Moosavi, Azam Amirian, Behnaz Zarbakhsh, Alireza Kordafshari, Hasan Mirzahoseini, Sirous Zeinali & Morteza Karimipoor. (2011) The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters. Hemoglobin 35:4, pages 323-330.
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Saedieh Ebrahimkhani, Azita Azarkeivan, Nooshin Bayat, Mahdieh Houry-Parvin, Sayeh Jalil-Nejad, Shima Zand, Zahra Golkar, Valeh Hadavi, Hashem Imanian, Christian Oberkanins & Hossein Najmabadi. (2011) Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease. Hemoglobin 35:1, pages 40-46.
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Azarkeivan Azita, Maryam Neishabury, Valeh Hadavi, Esteghamat Fatemehsadat, Saideh Enrahimkhani & Najmabadi Hossein. (2010) A REPORT OF 8 CASES WITH HEMOGLOBIN H DISEASE IN AN IRANIAN FAMILY. Pediatric Hematology and Oncology 27:5, pages 405-412.
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Valeh Hadavi, Maryam Jafroodi, Nima Hafezi-Nejad, Sousan Dehnadi Moghadam, Fatemeh Eskandari, Shahin Tarashohi, Hamideh Pourfahim, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutations in Gilan Province, North Iran. Hemoglobin 33:3-4, pages 235-241.
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Ahmad Tamaddoni, Valeh Hadavi, Nima Hafezi Nejad, Atefeh Khosh-Ain, Rita Siami, Jalil Aghai-Meibodi, Navid Almadani, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran. Hemoglobin 33:2, pages 115-123.
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Khodamorad Zandian, Jamal Nateghi, Bijan Keikhaie, Mohammad Pedram, Nima Hafezi-Nejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan, Hai-Yang Law & Hossein Najmabadi. (2008) α-Thalassemia Mutations in Khuzestan Province, Southwest Iran. Hemoglobin 32:6, pages 546-552.
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Babak Moghimi, Majid Yavarian, Christian Oberkanins, Seyyed Saeid Hosseini Amini, Shohreh Khatami, Soghra Rouhi, Kimia Kahrizi & Hossein Najmabadi. (2004) Hb Dhonburi (Neapolis) [β126(H4)Val→Gly] Identified in a Family from Northern Iran. Hemoglobin 28:4, pages 353-356.
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Articles from other publishers (7)

Jianjiang Feng, Di Cui, Caipeng Li, Yingsong Yang, Qiuli Li, Xiaomin Li, Shuming Tan, Zhiming Li, Wanli Meng, Haoxian Li & Yanghui Zhang. (2023) The comprehensive analysis of thalassemia alleles (CATSA) based on single-molecule real-time technology (SMRT) is a more powerful strategy in the diagnosis of thalassemia caused by rare variants. Clinica Chimica Acta 551, pages 117619.
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Mona Asghari Ahmadabad, Noushin Pourreza, Setareh Ramezanpour, Adel Baghersalimi, Mersedeh Enshaei, Marjan Askari, Amirhossein Alizadeh, Elahe Izadi & Bahram Darbandi. (2023) An analysis of the distribution and spectrum of alpha thalassemia mutations in Rasht City, North of Iran. Frontiers in Pediatrics 11.
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Sisi Ning, Yudi Luo, Yi Liang, Yuling Xie, Yinghong Lu, Binrong Meng, Jinjie Pan, Ruofan Xu, Yinyin Liu & Yunrong Qin. (2022) A novel rearrangement of the α-globin gene cluster containing both the −α3.7 and ααααanti4.2 crossover junctions in a Chinese family. Clinica Chimica Acta 535, pages 7-12.
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Mohammad-Sadegh Fallah, Reza Mahdian, Seyyed-Ahmad Aleyasin, Somayeh Jamali, Mina Hayat-Nosaeid, Moretza Karimipour, Marzieh Raeisi & Sirous Zeinali. (2010) Development of a quantitative real-time PCR assay for detection of unknown α-globin gene deletions. Blood Cells, Molecules, and Diseases 45:1, pages 58-64.
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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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Mohammad-Sadegh Fallah, Azita Zadeh-Vakili, Seyed-Ahmad Aleyasin, Reza Mahdian, Moretza Karimipour, Marzieh Raeisi, Somayeh Jamali, Ahmad Ebrahimi, Panti Fooladi, Majid Naderi, Erol Baysal & Sirous Zeinali. (2009) Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 β-thalassemia. Blood Cells, Molecules, and Diseases 43:2, pages 158-160.
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Zohreh Rahimi, Reza Akramipour, Asad Vaisi-Raygani, Ronald L. Nagel & Adriana Muniz. (2007) An Iranian Child With HbQ-Iran [α75 (EF4) Asp→His]/−α3.7 kb/IVSII.1 G→A. Journal of Pediatric Hematology/Oncology 29:9, pages 649-651.
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