Alpha globin gene duplications in beta thalassemia patients with intact beta globin gene
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference8 articles.
1. Thalassemia-like carriers not linked to the β-globin genes;Faá;Br. J. Haematol.,2006
2. Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients;Harteveld;Blood Cells Mol. Dis.,2008
3. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α-and β-thalassemia characterised by high resolution multiplex ligation-dependent probe amplification;Harteveld;J. Med. Genet.,2005
4. MLPA and MAPH: new techniques for detection of gene deletions;Sellner;Hum. Mutat.,2004
5. Genome-wide association study shows BCL11A associated with persistent fetal haemoglobin and amelioration of the phenotype of β-thalassemia;Uda;Proc. Natl. Acad. Sci. U. S. A.,2008
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. Missed Diagnosis of α-Globin Gene Cluster Duplication in Prenatal Screening: Identified Incidentally by Invasive Testing;Indian Journal of Hematology and Blood Transfusion;2022-01-20
2. Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child;Pediatric Hematology and Oncology;2015-06-18
3. The Prevention of Thalassemia;Cold Spring Harbor Perspectives in Medicine;2013-02-01
4. Modifier genes in Mendelian disorders: the example of hemoglobin disorders;Annals of the New York Academy of Sciences;2010-10-29
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