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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 3
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Original Article

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

Samaneh FarashiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran, ;Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran,
,
Negin Faramarzi GarousKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran,
,
Fatemeh ZeinaliKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran,
,
Shadi VakiliKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran,
,
Mehri AshkiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran,
,
Hashem ImanianKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran,
,
Hossein NajmabadiKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran, ;Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran,
,
Azita AzarkeivanKariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran, ;Thalassemia Clinic, Transfusion Research Center Organization, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
&
Ahmad TamaddoniBabol University of Medical Sciences, Babol, IranCorrespondence[email protected]
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Pages 196-200 | Received 06 May 2014, Accepted 24 Oct 2014, Published online: 15 May 2015

Citations (2)

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Read on this site (1)

Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Articles from other publishers (1)

Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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