Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

The hematological phenotypes of several Mediterranean patients with delta beta-thalassemia and hereditary persistence of fetal hemoglobin have been characterized. Although clinical and hematological characteristics are essentially superimposable in all heterozygous delta beta-thalassemics, these pat...

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Detalhes bibliográficos
Main Authors: Ottolenghi, S, Giglioni, B, Taramelli, R, Comi, P, Mazza, U, Saglio, G, Camaschella, C, Izzo, P, Cao, A, Galanello, R, Gimferrer, E, Baiget, M, Gianni, A M
Formato: Artigo
Idioma:Inglês
Publicado em: 1982
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC346190/
https://ncbi.nlm.nih.gov/pubmed/6179097
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