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Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease.

Interaction with the alpha-thalassaemia phenotypes lowers the proportion of Hb S in the sickle cell trait and influences the mean cell volume and proportional Hb A2 in homozygous sickle cell (SS) disease. By assigning somewhat arbitrary values to the alpha-thalassaemia 1 and alpha-thalassaemia 2 phe...

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Bibliografski detalji
Glavni autori: Serjeant, G R, Mason, K P, Serjeant, B E
Format: Artigo
Jezik:Inglês
Izdano: 1980
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048570/
https://ncbi.nlm.nih.gov/pubmed/7205903
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