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Beta-globin gene cluster haplotype effect on the clinical manifestation of sickle cell disease in Lebanon - by Wissam Ali Abou Alaiwi

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dc.contributor.author Abou Alaiwi, Wissam Ali
dc.date.accessioned 2012-06-13T07:05:55Z
dc.date.available 2012-06-13T07:05:55Z
dc.date.issued 2002
dc.identifier.uri http://hdl.handle.net/10938/6293
dc.description Thesis (M.S.)--American University of Beirut.Department of Biology, 2001;"Advisor: Dr. Elias Baydoun, Professor, Biology--Member of Committee: Dr. Pierre Zalloua. Assistani Professor, Saint Joseph University Chronic Care Center, Hazmieh--Member of Committ
dc.description Bibliography : leaves 74-79
dc.description.abstract In Africa, the p-globin gene cluster haplotypes may be associated with variable levels of Mb F, and hence, variable clinical and hematological features in patients with sickle cell disease (SS). The predominance of haplotype heterozygotes, and other influ
dc.format.extent xiv, 79 leaves : ill., tables
dc.language.iso eng
dc.relation.ispartof Theses, Dissertations, and Projects
dc.subject.classification T:004224 AUBNO
dc.subject.lcsh Sickle cell anemia -- Lebanon -- Case studies
dc.subject.lcsh Globin genes -- Case studies
dc.subject.lcsh Hemoglobin -- Synthesis -- Case studies
dc.subject.lcsh Thalassemia -- Lebanon -- Case studies
dc.title Beta-globin gene cluster haplotype effect on the clinical manifestation of sickle cell disease in Lebanon - by Wissam Ali Abou Alaiwi
dc.type Thesis
dc.contributor.department American University of Beirut. Faculty of Arts and Sciences. Department of Biology


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