The 12.6 kb-deletion in the -globin gene cluster is the known Thai/Vietnamese ( )0-thalassemia commonly found in Southeast Asia
Author:
Publisher
Ferrata Storti Foundation (Haematologica)
Subject
Hematology
Cited by 5 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. Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania;BMC Medical Genetics;2020-06-05
2. Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency?;Hemoglobin;2019-01-02
3. Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion;Taiwanese Journal of Obstetrics and Gynecology;2018-06
4. Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization;The Journal of Molecular Diagnostics;2016-01
5. Low fetal hemoglobin rates in patients carrying Thai ( )0-deletion and Turkish ( )0-deletion/inversion strengthen the hypothesis that the 5' BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to "The 12.6 kb-deletion in the -globin gene cluster is the known Thai/Vietnamese ( )0-thalassemia commonly found in Southeast Asia";Haematologica;2013-09-01
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