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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 1
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Original Article

Molecular Basis of Hb H Disease in Southwest Iran

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Pages 43-50 | Received 15 Jul 2004, Accepted 19 Aug 2004, Published online: 07 Jul 2009

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Hassan Abolghasemi, Sharareh Kamfar, Azita Azarkeivan, Mehran Karimi, Bijan Keikhaei, Fahimeh Abolghasemi, Mohammad H. Radfar, Peyman Eshghi & Samin Alavi. (2022) Clinical and genetic characteristics of hemoglobin H disease in Iran. Pediatric Hematology and Oncology 39:6, pages 489-499.
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Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali. (2020) α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. Hemoglobin 44:1, pages 20-26.
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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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Haleh Akhavan-Niaki, Ali Banihashemi, Amrollah Mostafazadeh, Vahid Kholghi Oskooei, Mandana Azizi, Reza Youssefi Kamangar & Maryam Mitra Elmi. (2012) Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran. Hemoglobin 36:2, pages 124-130.
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Piero C. Giordano, Marjon H. Cnossen, Annemarie M.S. Joosten, Cees A.M. Jansen, Tineke E. Hakvoort, Margreet Bakker-Verweij, Sandra G.J. Arkesteijn, Peter van Delft, John S. Waye, Marelle J. Bouva & Cornelis L. Harteveld. (2010) Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening. Hemoglobin 34:4, pages 354-365.
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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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Nasir A.S. Al-Allawi, Ameer I.A. Badi, Hasham Imanian, Nooshin Nikzat, Jaladet M.S. Jubrael & Hossein Najmabadi. (2009) Molecular Characterization of α-Thalassemia in the Dohuk Region of Iraq. Hemoglobin 33:1, pages 37-44.
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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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Articles from other publishers (4)

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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A. Zorai, I. Moumni, I. Mosbahi, K. Douzi, D. Chaouachi, F. Guemira & S. Abbes. (2015) Rare hemoglobin variants in Tunisian population. International Journal of Laboratory Hematology 37:2, pages 148-154.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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P. C. Giordano, A. Plancke, C. A. Van Meir, C. A. H. Janssen, P. J. M. J. Kok, I. H. Van Rooijen-Nijdam, B. C. Tanis, J. C. M. van Huisseling & F. G. A. Versteegh. (2006) Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study. Prenatal Diagnosis 26:8, pages 719-724.
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