The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1984.tb02229.x/fullpdf
Reference37 articles.
1. Evidence for multiple structural genes for the γ chain of human fetal hemoglobin;Schroeder;Proc Natl Acad Sci USA,1968
2. The present status of the heterogeneity of observations in thalassemia and related conditions;Huisman;Ann N Y Acad Sci USA,1974
3. The chemical heterogeneity of the foetal haemoglobin of Black newborn babies and adults: a reevaluation;Huisman;Blood,1981
4. Quantitation of three types of γ chain of the Hb F by high pressure liquid chromatography; application of this method to the Hb F of patients with sickle cell anaemia or the S-HPFH condition;Huisman;Blood,1981
5. The gamma chain heterogeneity of foetal haemoglobin in Black β-thalassaemia and HPFH hetero-zygotes;Huisman;Blood,1981
Cited by 3 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. Hémoglobinopathie O Arab homozygote dans une famille marocaine;Immuno-analyse & Biologie Spécialisée;2012-10
2. Structural Characterization of the β-Globin Gene Cluster in An Individual Expressing A Very Low Ll ofGγ Globin Chains;Hemoglobin;1995-01
3. Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O-Arab (β121[GH4]Glu→Lys) in a Moroccan man;American Journal of Hematology;1988-04
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