Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya
Author:
Publisher
Wiley
Subject
Hematology
Reference7 articles.
1. Hb S/β°-Thalassemia due to the ˜1.4-kb deletion is associated with a relatively mild phenotype
2. Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition
3. Hemoglobin Kenya, the product of fusion of γ and β polypeptide chains
4. Ion Transport in Plants
Cited by 6 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. Hemoglobin variants identified in the Uganda Sickle Surveillance Study;Blood Advances;2016-11-22
2. Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan Woman;Hemoglobin;2012-03-02
3. Hemoglobin Kenya composed of α- and (Aγβ)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin;American Journal of Hematology;2009-01
4. Multiplex-PCR Assay for the Deletions Causing Hereditary Persistence of Fetal Hemoglobin;Molecular Diagnosis;2005-09
5. IDENTIFICATION OF Hb KENYA (Aγ81Leu-β86Ala) BY ELECTROSPRAY MASS SPECTROMETRY;Hemoglobin;2002-01
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