Found: 3
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Case Report: α-Spectrin Mutation Associated with αLELY Polymorphism Responsible for Hereditary Pyropoikilocytosis.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
A Newborn Screening Program for Sickle Cell Disease in Murcia (Spain).
- Published in:
- International Journal of Neonatal Screening (IJNS), 2023, v. 9, n. 4, p. 55, doi. 10.3390/ijns9040055
- By:
- Publication type:
- Article
Flow Cytometry as a New Accessible Method to Evaluate Diagnostic Osmotic Changes in Patients with Red Blood Cell Membrane Defects.
- Published in:
- Biomedicines, 2024, v. 13, n. 7, p. 1607, doi. 10.3390/biomedicines12071607
- By:
- Publication type:
- Article