Haematological Characterisation and Molecular Basis of Asian Indian Inversion Deletions Delta Beta Thalassemia: A Case Report

The hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia are heterogeneous disorders characterised by increased levels of fetal hemoglobin and high level of this Hb continues in adulthood. The distinction between these two conditions is not always possible with routine hemato...

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Detalles Bibliográficos
Publicado en:J Clin Diagn Res
Autores principales: Khunger, Jitender Mohan, Gupta, Monika, Singh, Rekha, Kapoor, Rohit, Pandey, Hare Ram
Formato: Artigo
Lenguaje:Inglês
Publicado: JCDR Research and Publications (P) Limited 2014
Materias:
Pathology Section
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4225894/
https://ncbi.nlm.nih.gov/pubmed/25386442
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2014/8362.4776
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