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.authorAbou Alaiwi, Wissam Ali
dc.contributor.departmentDepartment of Biology
dc.contributor.facultyFaculty of Arts and Sciences
dc.contributor.institutionAmerican University of Beirut
dc.date2002
dc.date.accessioned2012-06-13T07:05:55Z
dc.date.available2012-06-13T07:05:55Z
dc.date.issued2002
dc.descriptionThesis (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.descriptionBibliography : leaves 74-79
dc.description.abstractIn 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.extentxiv, 79 leaves : ill., tables
dc.identifier.urihttp://hdl.handle.net/10938/6293
dc.language.isoen
dc.relation.ispartofTheses, Dissertations, and Projects
dc.subject.classificationT:004224 AUBNO
dc.subject.lcshSickle cell anemia -- Lebanon -- Case studies
dc.subject.lcshGlobin genes -- Case studies
dc.subject.lcshHemoglobin -- Synthesis -- Case studies
dc.subject.lcshThalassemia -- Lebanon -- Case studies
dc.titleBeta-globin gene cluster haplotype effect on the clinical manifestation of sickle cell disease in Lebanon - by Wissam Ali Abou Alaiwi
dc.typeThesis

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