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Observations on the high foetal haemoglobin gene and its interaction with the thalassaemia gene

A family of mixed Indian-Portuguese ancestry is reported in which there is a hereditary persistence of foetal haemoglobin and β-chain thalassaemia. The propositus, a 17-year-old boy, was found to have a mild haemolytic anaemia characterized by slight splenomegaly, microcytosis, numerous target cells...

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Hlavní autoři: Barkhan, P., Adinolfi, M.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1962
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC480412/
https://ncbi.nlm.nih.gov/pubmed/13865031
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