Molecular spectrum and distribution of hemoglobinopathies in southwest of Iran: a seven-year retrospective study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,Histology,Pathology and Forensic Medicine
Link
http://link.springer.com/content/pdf/10.1007/s12308-020-00388-7.pdf
Reference46 articles.
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3. Mettananda S, Higgs DR (2018) Molecular basis and genetic modifiers of thalassemia. Hematol Oncol Clin North Am 32(2):237–245
4. Harteveld CL et al (2010) Α-thalassaemia. Orphanet J Rare Dis 5(1):13
5. Al-Amodi AM et al (2018) Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT). Curr Med Res Opin
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1. Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients;Hemoglobin;2020-03-03
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