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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Davies, S, Henthorn, J, Brozović, M
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1983
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC498461/
https://ncbi.nlm.nih.gov/pubmed/6886017
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