Haemoglobin Bart's hydrops syndrome in Greece.

A case of haemoglobin Bart's hydrops syndrome was characterised in a Greek family with a history of three other fetuses with hydrops. Family studies showed that both the mother and father carried alpha-thalassaemia genes, and globin-chain synthesis analysis of the present fetus showed a total a...

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Detalhes bibliográficos
Main Authors: Kattamis, C, Metaxotou-Mavromati, A, Tsiarta, E, Metaxatou, C, Wasi, P, Wood, W G, Pressley, L, Higgs, D R, Clegg, J B, Weatherall, D J
Formato: Artigo
Idioma:Inglês
Publicado em: 1980
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1713863/
https://ncbi.nlm.nih.gov/pubmed/7427238
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