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Updated: Feb 23, 2026

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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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Sickle cell trait with β-thalassemia, elliptocytosis, and thrombocytosis
Jamie L Lombardo1, David T Lynch1
1San Antonio Military Medical Center.
Blood
|September 9, 2017
Abstract
No abstract available in PubMed .
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