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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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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. (2010) Correlation of beta-thalassemia mutations with alpha-thalassemia: an experience of the southwestern region of Iran. Hematology 15:6, pages 430-433.
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Mohammad Ali Ehsani, Amir Abbas Hedayati-Asl, Alireza Bagheri, Syrus Zeinali & Armin Rashidi. (2009) HYDROXYUREA-INDUCED HEMATOLOGICAL RESPONSE IN TRANSFUSION-INDEPENDENT BETA-THALASSEMIA INTERMEDIA: Case Series and Review of Literature. Pediatric Hematology and Oncology 26:8, pages 560-565.
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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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Imane Agouti, Mohcine Bennani, Nicolas Levy, Piero Giordano & Catherine Badens. (2009) The Rare Codon 24 (T>A) (β+) Mutation in Association with the Common Codon 39 (C> T) (β0) Mutation Causes Transfusion-Dependent β-Thalassemia in a Moroccan Patient. Hemoglobin 33:2, pages 150-154.
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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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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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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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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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Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2005) A Mutation of the β-Globin Gene Initiation Codon, ATG→AAG, Found in a French Caucasian Man. Hemoglobin 29:3, pages 225-228.
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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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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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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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Articles from other publishers (8)
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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Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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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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V. VIPRAKASIT, W. CHINCHANG, L. SUWANTHOL & V. S. TANPHAICHITR. (2005) Common origin of a rare beta-globin initiation codon mutation (ATGAGG) in Asians. Clinical and Laboratory Haematology 27:6, pages 409-415.
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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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