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The Diagnosis of α-Thalassaemia: A Case of Hemoglobin H −α(3.7) Deletion
We report a case of hemolytic anemia that was subsequently identified to be a case of α-thalassaemia harboring the common rightward 3.7 kb deletion/HbH. The diagnosis was based on sequential analyses using BioRad D10 HPLC, Alkaline gel electrophoresis, GPO α THAL-IC strips and the identification of...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2994557/ https://ncbi.nlm.nih.gov/pubmed/21966120 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12291-010-0053-7 |
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