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Phenotype-genotype correlation in haemoglobin H disease in childhood.

In this study we used restriction endonuclease mapping to characterise the molecular defect responsible for haemoglobin H disease in 14 Sardinian children. The resulting genotypes were then correlated with the respective clinical and haematological phenotypes. We found that patients with the combina...

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Bibliografski detalji
Glavni autori: Galanello, R, Pirastu, M, Melis, M A, Paglietti, E, Moi, P, Cao, A
Format: Artigo
Jezik:Inglês
Izdano: 1983
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049173/
https://ncbi.nlm.nih.gov/pubmed/6317863
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