Triplication (/???Anti3.7) or deletion (-?3.7/) association in Argentinian ?-thalassemic carriers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-003-0738-6.pdf
Cited by 12 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. Detection of −α 3.7 and _ _SEA deletions in α-globin gene in the Bangladeshi population;2024-01-03
2. Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual;eJHaem;2021-07-19
3. The carriage rates of αααanti3.7, αααanti4.2, and HKαα in the population of Guangxi, China measured using a rapid detection qPCR system to determine CNV in the α-globin gene cluster;Gene;2021-02
4. Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian Population;Hemoglobin;2018-07-04
5. The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population;Molecular Medicine Reports;2017-11-13
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