Found: 4
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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
Effects of imipramine on cancer patients over-expressing Fascin1; description of the HITCLIF clinical trial.
- Published in:
- Frontiers in Oncology, 2024, p. 01, doi. 10.3389/fonc.2023.1238464
- By:
- Publication type:
- Article
Effects of imipramine on cancer patients over-expressing Fascin1; description of the HITCLIF clinical trial.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2023.1238464
- By:
- Publication type:
- Article