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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 5
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Original Article

Comprehensive Spectrum of the β-Thalassemia Mutations in Khuzestan, Southwest Iran

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Pages 461-468 | Received 17 Mar 2010, Accepted 04 May 2010, Published online: 20 Sep 2010

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Read on this site (5)

Niloofar Bazazzadegan, Seyedeh Sedigheh Abedini, Azita Azarkeivan, Susan Banihashemi, Nooshin Nikzat, Hossein Najmabadi & Maryam Neishabury. (2023) The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran. Hemoglobin 47:4, pages 147-151.
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Keivan Moradi, Mozaffar Aznab, Susan Tahmasebi, Leila Omidniakan, Nushin Bijari & Reza Alibakhshi. (2020) Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West Iran. Hemoglobin 44:4, pages 244-248.
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Reza Alibakhshi, Keivan Moradi, Mozaffar Aznab, Azam Azimi, Samaneh Shafieenia & Mostafa Biglari. (2019) The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran. Hemoglobin 43:1, pages 18-22.
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Leila Jamali, Mohammad Mehdi Banoei, Elham Khalili, Sepideh Dadgar & Massoud Houshmand. (2016) Association of genetic variations in the mitochondrial D-loop with β-thalassemia. Mitochondrial DNA Part A 27:3, pages 1693-1696.
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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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Articles from other publishers (9)

Sahand Khamooshian, Mohsen Kazeminia & Keivan Moradi. (2022) In silico analysis and the pathogenicity classification of PTS gene variants among Iranian population. Egyptian Journal of Medical Human Genetics 23:1.
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Hamid Galehdari, Mehdi Bijanzadeh, Seyedeh Zohreh Azarshin, Mohammad Shafee & Sogand Heydaran. (2021) Design and Development of Reverse Slot Blot for the Simultaneous Detection of Rare and Regional Specific Mutations in the Beta Globin Gene in Khuzestan Province of Iran. Indian Journal of Hematology and Blood Transfusion 37:3, pages 436-441.
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Fatemeh Asadi, Seyedeh Moloud Rasouli Ghahfarokhi & Forough Talebi. (2019) Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran. Medical Laboratory Journal 13:2, pages 48-54.
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Somaye Heidari sharafdarkolaee, Majid Motovali-Bashi & Pooria Gill. (2018) The sensitive detection of IVSII-1(G˃A) mutation in beta globin gene using a Nano-based ligation genotyping system. Gene 674, pages 98-103.
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Masoomeh Sayahi, Farideh Ghanbari Mardasi & Masoomeh Salehi Kambo. (2017) Thalassemia Spectrum and Prenatal Diagnosis among Voluntary Couples in Shushtar City, during a Five Year Period. Gene, Cell and Tissue 4:4.
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Nejat Mahdieh & Bahareh Rabbani. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews 30:6, pages 493-508.
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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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Haleh Akhavan-NiakiSiamak Shafiezadeh SerestiBeheshteh AsghariAli Banihashemi. (2011) IVSII-666 of Human Beta-Globin Gene: A Polymorphic Marker Linked to Codon 8(-AA) Mutation. Genetic Testing and Molecular Biomarkers 15:7-8, pages 573-576.
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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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