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Updated: Mar 20, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Interaction between hereditary spherocytosis and the beta-thalassemia trait: A case report
Sunita Sharma1, Sonal Jain Malhotra, Richa Chauhan
1Department of Pathology, Lady Hardinge Medical College, Delhi University, 110001 New Delhi, India Phone: (91)0120-2554266
No abstract available in PubMed .
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