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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: Bhat, Vijay S., Dewan, Kalyan Kumar, Krishnaswamy, Patnam Rajagopalan
Formáid: Artigo
Teanga:Inglês
Foilsithe: Springer-Verlag 2010
Ábhair:
Rochtain Ar Líne: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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