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pubmed-article:8104463pubmed:abstractTextWe report here on the final results of an epidemiological survey involving 177 beta-thalassaemic chromosomes in Algeria. Four common mutations account for 86% of the chromosomes, the other ones carrying nine other rare mutations. Combination of these results with those of other smaller regional epidemiological studies indicates the existence of still a wider range of mutations. The nature and frequencies of these mutations, their linkage with RFLP-haplotypes, agree well with the history of the region. Knowledge of this spectrum of mutations enables the design of a diagnosis strategy that takes into account the local economical constraints.lld:pubmed
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pubmed-article:8104463pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8104463pubmed:year1993lld:pubmed
pubmed-article:8104463pubmed:articleTitleThe spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy.lld:pubmed
pubmed-article:8104463pubmed:affiliationCentre de Transfusion Sanguine, Hôpital Mustapha, Alger, Algérie.lld:pubmed
pubmed-article:8104463pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8104463pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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