Co-inheritance of haemoglobin A2 and beta-thalassaemia in cis
Author:
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Reference11 articles.
1. Origin of Hb A2 (Hb B2) [delta16(A13)GlyArg (GGCCGC)];Bennani;Hemoglobin,2003
2. Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant;Codrington;Blood,1990
3. Identification of hemoglobin variants by HPLC;Hoyer;Clinical Chemistry,2005
4. Thalassemia minor associated with hemoglobin-B2 heterozygosity. A family report;Huisman;Blood,1961
5. Structural characterization of two delta chain variants;Jones;Journal of Biological Chemistry,1967
Cited by 4 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. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2Sample;Hemoglobin;2019-01-02
2. Heterozygous β-thalassemia with complete absence of hemoglobin A2in a Chinese adult;International Journal of Laboratory Hematology;2015-06-11
3. Normal Hb A2β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) inCiswith the Hb A2’δ-Globin Gene Missense Mutation (HBD: c.49G>C);Hemoglobin;2013-02-11
4. An insight into the suspected HbA2' cases detected by high performance liquid chromatography in Pakistan;BMC Research Notes;2011-04-05
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