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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 5
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Original Article

A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor

Tahereh ZareiHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran;
,
Javad DehbozorgianHematology Research Center, Dastgheib Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
,
Jaber ImanifardHematology Research Center, Dastgheib Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
,
Fatemehsadat SetoodeganHematology Research Center, Dastgheib Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
&
Mehran KarimiHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Correspondence[email protected]
Pages 316-318 | Received 23 May 2016, Accepted 12 Jul 2016, Published online: 22 Sep 2016

Citations (2)

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Read on this site (1)

Gui-Lan Chen, Fan Jiang, Jian Li, Jian-Ying Zhou & Dong-Zhi Li. (2018) Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients. Hemoglobin 42:5-6, pages 306-309.
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Articles from other publishers (1)

Hou Qian, Jianlin Huang, Ji Xu, Weihua Zhao, Xiufeng Ye & Wenlan Liu. (2020) Prenatal diagnosis of a rare β ‐thalassemia gene －90 (C>T) ( HBB : c.‐140 C>T) mutation associated with deletional Hb H disease (‐‐ SEA /‐ α 4.2 ) . Molecular Genetics & Genomic Medicine 8:11.
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