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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
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MOLECULAR SPECTRUM OF β-THALASSEMIA IN THE IRANIAN PROVINCE OF HORMOZGAN

Majid Yavarian The Thalassemia Medical Centre, Medical Faculty, Pasture Laboratory, Bandar Abbas University, Bandar Abbas, Iran
,
Cees L. Harteveld Department of Human and Clinical Genetics, Hemoglobinopathies Laboratory, Leiden University Medical Centre, 2333, AL, Leiden, The Netherlands
,
Desiree Batelaan Department of Human and Clinical Genetics, Hemoglobinopathies Laboratory, Leiden University Medical Centre, 2333, AL, Leiden, The Netherlands
,
Luigi F. Bernini Department of Human and Clinical Genetics, Hemoglobinopathies Laboratory, Leiden University Medical Centre, 2333, AL, Leiden, The Netherlands
&
Piero C. Giordano Department of Human and Clinical Genetics, Hemoglobinopathies Laboratory, Leiden University Medical Centre, 2333, AL, Leiden, The Netherlands; Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Centre, Wassenaarseweg 72, 2333, AL, Leiden, The Netherlands
Pages 35-43 | Received 03 Mar 2000, Accepted 31 Jul 2000, Published online: 07 Jul 2009

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Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
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Suha M. Hassan, Cornelis L. Harteveld, Egbert Bakker & Piero C. Giordano. (2015) Broader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries. Hemoglobin 39:2, pages 107-110.
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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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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. (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 Saeid Rahiminejad, Sirous Zeinali, Abdolreza Afrasiabi & Ali Kord Valeshabad. (2011) β-Thalassemia Mutations Found During 1 Year of Prenatal Diagnoses in Fars Province, Iran. Hemoglobin 35:4, pages 331-337.
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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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Majid Yavarian, Mehran Karimi, Farideh Paran, Catherine Neven, Cornelis L. Harteveld & Piero C. Giordano. (2009) Multi Centric Origin of Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA]. Hemoglobin 33:6, pages 399-405.
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Azita Zadeh-Vakili & Payman Eshghi. (2009) Detection of a Rare Mutation in An Iranian Family: Codons 37/38/39 (7 bp Deletion). Hemoglobin 33:6, pages 523-527.
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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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Danny C. Liaw, Adam Kotkiewicz & Mark A. Kender. (2009) Acute Splenic Infarct in β-Thalassemia Minor: A Novel Combination of Heterozygous β-Globin Mutations with Latent Phenotypes and the Clinical Implications. Hemoglobin 33:3-4, pages 262-268.
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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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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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Pooneh Nikuei, Valeh Hadavi, Minoo Rajaei, Mozhgan Saberi, Fozieh Hajizade & Hossein Najmabadi. (2008) Prenatal Diagnosis for β-Thalassemia Major in the Iranian Province of Hormozgan. Hemoglobin 32:6, pages 539-545.
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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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Mohammad A. Hosseinpour Feizi, Abbas A. Hosseinpour Feizi, Nasser Pouladi, Mehdi Haghi & Parvin Azarfam. (2008) Molecular Spectrum of β-Thalassemia Mutations in Northwestern Iran. Hemoglobin 32:3, pages 255-261.
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Peyman Eshghi, Azita Zadeh-Vakili, Armin Rashidi & Ebrahim Miri-Moghadam. (2008) An Unusually Frequent β-Thalassemia Mutation in an Iranian Province. Hemoglobin 32:4, pages 387-392.
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Fatemehsadat Esteghamat, Hashem Imanian, Azita Azarkeivan, Farzin Pourfarzad, Navid Almadani & Hossein Najmabadi. (2007) Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster. Hemoglobin 31:4, pages 463-469.
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Ishwar C. Verma, Marina Kleanthous, Renu Saxena, Suthat Fucharoen, Pranee Winichagoon, Sheikh Raizuddin, Shaheen N. Khan, Mohammad T. Akbari, Mina Izadyar, Navratnam Kotea, John M. Old, Panayiotis A. Ioannou & Baldip Khan. (2007) Multicenter Study of the Molecular Basis of Thalassemia Intermedia in Different Ethnic Populations. Hemoglobin 31:4, pages 439-452.
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Pupak Derakhshandeh-Peykar, Haleh Akhavan-Niaki, Ahmad Tamaddoni, Shohreh Ghawidel-Parsa, Kourosh Holakouie Naieni, Manijeh Rahmani, Farbod Babrzadeh, Mohammad Dilmaghani-Zadeh & Dariush Daneshvar Farhud. (2007) Distribution of β-Thalassemia Mutations in the Northern Provinces of Iran. Hemoglobin 31:3, pages 351-356.
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Ali Asghar Kiani, Yousef Mortazavi, Sirous Zeinali & Yaghob Shirkhani. (2007) The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran. Hemoglobin 31:3, pages 343-349.
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Laura Cremonesi, Maurizio Ferrari, Piero C. Giordano, Cornelis L. Harteveld, Marina Kleanthous, Thessalia Papasavva, George P. Patrinos & Joanne Traeger-Synodinos. (2007) An Overview of Current Microarray-Based Human Globin Gene Mutation Detection Methods. Hemoglobin 31:3, pages 289-311.
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Aisha Al-Obaidli, Mowafak Hamodat, Zainab Fawzi, Mohamed Abu-Laban, Nathalie Gerard & Rajagopal Krishnamoorthy. (2007) Molecular Basis of Thalassemia in Qatar. Hemoglobin 31:2, pages 121-127.
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Amina Bibi, Taieb Messaoud & Slaheddine Fattoum. (2006) Haplotypes Linked to Three Rare β-Thalassemia Mutations, Originally Reported in Tunisia. Hemoglobin 30:2, pages 175-181.
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Mehran Karimi, Hooman Yarmohammadi, Shirin Farjadian, Sirus Zeinali, Zahra Moghaddam, Maria D. Cappellini & Piero C. Giordano. (2002) β-THALASSEMIA INTERMEDIA FROM SOUTHERN IRAN: IVS-II-1 (G→A) IS THE PREVALENT THALASSEMIA INTERMEDIA ALLELE. Hemoglobin 26:2, pages 147-154.
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