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Page 1
Hematologic features of alpha thalassemia carriers.
Int J Mol Cell Med. 2012 Summer;1(3):162-7.
Int J Mol Cell Med. 2012.
PMID: 24551772
Free PMC article.
Beta globin frameworks in thalassemia major patients from north iran.
Akhavan-Niaki H, Banihashemi A, Azizi M.
Akhavan-Niaki H, et al. Among authors: azizi m.
Iran J Pediatr. 2012 Sep;22(3):297-302.
Iran J Pediatr. 2012.
PMID: 23399541
Free PMC article.
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Coinheritance of Sicilian (δβ)0-Thalassemia and Two Rare Hemoglobin Variants: A Complex Case of Hemoglobinopathy.
Eftekhari H, Pilehchian Langroudi M, Banihashemi A, Azizi M, Kamangar RY, Akhavan-Niaki H.
Eftekhari H, et al. Among authors: azizi m.
Indian J Clin Biochem. 2018 Apr;33(2):231-234. doi: 10.1007/s12291-017-0676-z. Epub 2017 Jul 5.
Indian J Clin Biochem. 2018.
PMID: 29651217
Free PMC article.
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A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population.
Akhavan-Niaki H, Derakhshandeh-Peykar P, Banihashemi A, Mostafazadeh A, Asghari B, Ahmadifard MR, Azizi M, Youssefi A, Elmi MM.
Akhavan-Niaki H, et al. Among authors: azizi m.
Blood Cells Mol Dis. 2011 Jun 15;47(1):29-32. doi: 10.1016/j.bcmd.2011.03.005. Epub 2011 Apr 13.
Blood Cells Mol Dis. 2011.
PMID: 21493114
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A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran.
Eftekhari H, Tamaddoni A, Mahmoudi Nesheli H, Vakili M, Sedaghat S, Banihashemi A, Azizi M, Youssefi Kamangar R, Akhavan-Niaki H.
Eftekhari H, et al. Among authors: azizi m.
Hemoglobin. 2017 Jan;41(1):32-37. doi: 10.1080/03630269.2017.1299753. Epub 2017 Apr 7.
Hemoglobin. 2017.
PMID: 28385057
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Identification of a Rare β(0)-Thalassemia Mutation, Codon 54 (-T) (HBB: c.165delT) in an Iranian Family.
Ghasemian Dastjerdy N, Banihashemi A, Azizi M, Akhavan-Niaki H.
Ghasemian Dastjerdy N, et al. Among authors: azizi m.
Hemoglobin. 2015;39(6):445-7. doi: 10.3109/03630269.2015.1071269. Epub 2015 Aug 19.
Hemoglobin. 2015.
PMID: 26290442
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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.
Akhavan-Niaki H, Banihashemi A, Mostafazadeh A, Kholghi Oskooei V, Azizi M, Youssefi Kamangar R, Elmi MM.
Akhavan-Niaki H, et al. Among authors: azizi m.
Hemoglobin. 2012;36(2):124-30. doi: 10.3109/03630269.2012.657728. Epub 2012 Feb 22.
Hemoglobin. 2012.
PMID: 22356652
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