Iron deficiency in sickle cell anaemia.
Thirty-seven patients with SCD were studied: 24 were diagnosed as homozygous Hb S on the basis of their haematological findings, and alpha:non-alpha globin chain ratios were found to be balanced in all. Thirteen patients were thought to have alpha or beta thalassaemia interaction with Hb S on the ba...
שמור ב:
| הוצא לאור ב: | J Clin Pathol |
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| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
1983
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC498461/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6886017/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jcp.36.9.1012 |
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