The molecular basis of B [Beta] -thalassaemia in Lebanon a reassessment - by Maya Abdul-Hamid Saleh

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6-Thalassaemia is an autosomal recessive genetic disorder of haemoglobin synthesis, concentrated in regions previously endemic for malaria, mainly the Mediterranean basin, the Middle-East, South-East Asia and parts of Africa. In Lebanon, it has been estim

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Thesis (M.S.) -- American University of Beirut. Department of Biology, 1995.;"Advisor: Rabih S. Talhouk, Assistant Professor, Molecular Biology -- Members of Committee: Leila F.. Zahed, Assistant Professor, Genetics Ghassan Matar, Assistant Professor, Mi
Bibliography: leaves 66-72.

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