Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 39 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. Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand;Scientific Reports;2024-04-22
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4. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28
5. Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent;Acta Haematologica;2020
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