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The molecular basis of B [Beta] -thalassaemia in Lebanon a reassessment - by Maya Abdul-Hamid Saleh
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| dc.contributor.author | Saleh, Maya Abdul-Hamid |
| dc.date.accessioned | 2012-06-13T06:42:48Z |
| dc.date.available | 2012-06-13T06:42:48Z |
| dc.date.issued | 1995 |
| dc.identifier.uri | http://hdl.handle.net/10938/5062 |
| dc.description | 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 |
| dc.description | Bibliography: leaves 66-72. |
| dc.description.abstract | 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 |
| dc.format.extent | xiii, 79 leaves : ill., mounted photographs. |
| dc.language.iso | eng |
| dc.relation.ispartof | Theses, Dissertations, and Projects |
| dc.subject.classification | T:003663 AUBNO |
| dc.subject.lcsh | Thalassemia -- Lebanon. |
| dc.title | The molecular basis of B [Beta] -thalassaemia in Lebanon a reassessment - by Maya Abdul-Hamid Saleh |
| dc.type | Thesis |
| dc.contributor.department | American University of Beirut. Faculty of Arts and Sciences. Department of Biology |
