Association of Low Serum Iron with Alpha Globin Gene Deletions and High Level of HbF with Xmn-1 Polymorphism in Sickle Cell Traits
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s12291-011-0170-y.pdf
Reference25 articles.
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3. Kanavakis E, Wainscoat JS, Wood WG, Weatherall DJ, Cao A, Furbetta M, et al. The intraction of alpha thalassemia with hetrozygus beta thalassemia. Br J Haematol. 1982;52(3):465–73.
4. Wainscoat JS, Kanavakis E, Wood WG, Letsky EA, Huehns ER, Marsh GW, Higgs DR, et al. Thalassemia intermedia in Cyprus: the interaction of alpha and beta thalassemia. Br J Haematol. 1983;53(3):411–6.
5. Gilman JG, Huisman THJ. DNA sequence variation associated with elevated fetal Gg globin production. Blood. 1985;66:783–7.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. XmnI Polymorphism in Sickle Cell Disease in North Morocco;Hemoglobin;2020-05-03
2. Association of Xmn1 −158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia;Molecular Biology Reports;2014-02-02
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