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Hemoglobin
international journal for hemoglobin research
Volume 18, 1994 - Issue 6
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Miscellaneous Article

β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm

M. R. Noori-Daloii Department o f Biochemistry, School of Medicine, Tehran University of Medical Sciences Tehran Islamic Republic, Iran
,
N. Moazami Department of Biotechnology, Iranian Research Organization for Science and Technology Tehran, Iran
,
S. Farhangi Queshm Island Medical Center Queshm, Iran
,
A. Atalay Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey
,
I. N. Geren Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey
,
L. Akar Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey
,
E. O. Atalay Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey
,
B. Clirakoglu Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey; Department of Medical Biology, Faculty of Medicine Marmara University, Haydarpasa, Istanbul, Turkey
&
E. Bermek Marmara Research Center Research Institute for Genetic Engineering and Biotechnology Gebze, Kocaeli, Turkey; Department of Biophysics, Istanbul University, Istanbul Faculty of Medicine Capa, Istanbul, Turkey
 show all
Pages 449-453 | Received 14 Jan 1994, Accepted 18 Oct 1994, Published online: 07 Jul 2009

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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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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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Fakher Rahim, Bijan Kaikhaei, Khodamorad Zandian & Ashraf Hoseini. (2008) Co-inheritance of α-and β-thalassemia in Khuzestan Province, Iran. Hematology 13:1, pages 59-64.
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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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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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Hossein Najmabadi, Roxana Karimi-Nejad, Solmaz Sahebjam, Farzin Pourfarzad, Shahram Teimourian, Farhad Sahebjam, Naser Amirizadeh & Mohammad H. Karimi-Nejad. (2001) THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION. Hemoglobin 25:3, pages 285-296.
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Majid Yavarian, Cees L. Harteveld, Desiree Batelaan, Luigi F. Bernini & Piero C. Giordano. (2001) MOLECULAR SPECTRUM OF β-THALASSEMIA IN THE IRANIAN PROVINCE OF HORMOZGAN. Hemoglobin 25:1, pages 35-43.
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C. Badens, N. Jassim, N. Martini, J. F. Mattei, J. Elion & D. Lena-Russo. (1999) Characterization of a New Polymorphism, IVS-I-108 (T→C), and a New β-Thalassemia Mutation, -27 (A→T), Discovered in the Course of a Prenatal Diagnosis. Hemoglobin 23:4, pages 339-344.
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G. Nozari, S. Rahbar, A. Golshaiyzan & S. Rahmanzadeh. (1995) Molecular Analyses of β-Thalassa in Iran. Hemoglobin 19:6, pages 425-431.
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Articles from other publishers (6)

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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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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Pooria Gill, Mehdi Forouzandeh, Naser Eshraghi, Mostafa Ghalami, Majid Safa & Mohammad-Reza Noori-Daloii. (2008) Detection of four β-thalassemia point mutations in Iranians using a PCR-ELISA genotyping system. Molecular and Cellular Probes 22:2, pages 103-109.
Crossref
Shahram Akhlaghpoor. (2006) Chorionic villus sampling for beta-thalassemia: the first report of experience in Iran. Prenatal Diagnosis 26:12, pages 1131-1136.
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Hossein Najmabadi, Maryam Neishabury, Farhad Sahebjam, Kimia Kahrizi, Yousef Shafaghati, Nushin Nikzat, Maryam Jalalvand, Farahnaz Aminy, Susan Bany Hashemi, Babak Moghimi, Ali Reza Noorian, Ali Jannati, Mehrdad Mohammadi & Khalil Javan. (2003) The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research. Human Mutation 21:2, pages 146-150.
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