Molecular Genetics of Thalassemia Syndromes
Author:
Publisher
Morgan & Claypool Publishers LLC
Subject
Automotive Engineering
Reference112 articles.
1. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb ?-globin gene deletion
2. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia
3. Detection of common deletional α-thalassemia-2 determinants by PCR
Cited by 2 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. β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases;International Journal of Laboratory Hematology;2023-02-22
2. Detection of BCL11A, HMIP, and XmnI polymorphisms among anemic pregnant women in hospital Universiti Sains Malaysia;Journal of Applied Hematology;2022
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