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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 4
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Original Article

Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster

Fatemehsadat Esteghamat Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran; Genetic Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
,
Hashem Imanian Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran
,
Azita Azarkeivan Blood Transfusion Organization, Research Center, Thalassemia Clinic, Tehran, Iran
,
Farzin Pourfarzad Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran
,
Navid Almadani Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran
&
Hossein Najmabadi Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran; Genetic Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranCorrespondence[email protected]; [email protected]
Pages 463-469 | Received 07 Aug 2006, Accepted 27 Jun 2007, Published online: 07 Jul 2009

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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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Anita Nadkarni, Marukh Wadia, Ajit Gorakshakar, Ryoiti Kiyama, Roshan B. Colah & Dipika Mohanty. (2008) Molecular Characterization of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population. Hemoglobin 32:5, pages 425-433.
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Articles from other publishers (2)

F.H. Abbasali, K.Sh. Mahmoud, N. Hengameh, D.H. Mina, D. Setare, D.M Hale & D.M. Sima. (2023) Rare and New Mutations of B-Globin in Azari Population of Iran, a Considerable Diversity. Balkan Journal of Medical Genetics 25:2, pages 51-62.
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Gargi Bhattacharya, Debasis Banerjee, Sarmila Chandra, Malay Ghosh, Utpal Chaudhuri, Manikanchan Das & Uma B. Dasgupta. (2008) Molecular basis of deletional hereditary persistence of fetal hemoglobin and δβ-thalassemia in Indian patients. Clinica Chimica Acta 392:1-2, pages 69-70.
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