A Rare Case of Compound Heterozygous Sickle Cell Beta Thalassaemia with High HbF and Normal HbA2 Levels Detected on HPLC.
| Autor: | AGARWAL, RUCHI1, HOODA, SUNAINA2, PARUL3 parul.smgs@gmail.com, SINGH, KULWANT1, THOMBRE, ADESH4 |
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| Zdroj: | Journal of Clinical & Diagnostic Research. May2024, Vol. 18 Issue 5, p14-17. 4p. |
| Databáze: | Academic Search Ultimate |
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