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postgraduate thesis: Detection of non-deletional mutations of {221} globin gene cluster in patients with unexplained {221} thalassaemia and hereditarypersistence of fetal haemoglobin

TitleDetection of non-deletional mutations of {221} globin gene cluster in patients with unexplained {221} thalassaemia and hereditarypersistence of fetal haemoglobin
Authors
Fung, Wai-kei, Vicky馮慧琪
Issue Date2010
PublisherThe University of Hong Kong (Pokfulam, Hong Kong)
Citation
Fung, W. V. [馮慧琪]. (2010). Detection of non-deletional mutations of β globin gene cluster in patients with unexplained β thalassaemia and hereditary persistence of fetal haemoglobin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4516060
DegreeMaster of Medical Sciences
SubjectThalassemia - Genetic aspects.
Hemoglobinopathy - Genetic aspects.
Globin genes.
Dept/ProgramPathology
Persistent Identifierhttp://hdl.handle.net/10722/132112
HKU Library Item IDb4516060

 

DC FieldValueLanguage
dc.contributor.authorFung, Wai-kei, Vicky-
dc.contributor.author馮慧琪-
dc.date.issued2010-
dc.identifier.citationFung, W. V. [馮慧琪]. (2010). Detection of non-deletional mutations of β globin gene cluster in patients with unexplained β thalassaemia and hereditary persistence of fetal haemoglobin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4516060-
dc.identifier.urihttp://hdl.handle.net/10722/132112-
dc.languageeng-
dc.publisherThe University of Hong Kong (Pokfulam, Hong Kong)-
dc.relation.ispartofHKU Theses Online (HKUTO)-
dc.rightsThe author retains all proprietary rights, (such as patent rights) and the right to use in future works.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.source.urihttp://hub.hku.hk/bib/B45160600-
dc.subject.lcshThalassemia - Genetic aspects.-
dc.subject.lcshHemoglobinopathy - Genetic aspects.-
dc.subject.lcshGlobin genes.-
dc.titleDetection of non-deletional mutations of {221} globin gene cluster in patients with unexplained {221} thalassaemia and hereditarypersistence of fetal haemoglobin-
dc.typePG_Thesis-
dc.identifier.hkulb4516060-
dc.description.thesisnameMaster of Medical Sciences-
dc.description.thesislevelMaster-
dc.description.thesisdisciplinePathology-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.5353/th_b4516060-
dc.date.hkucongregation2010-
dc.identifier.mmsid991031034879703414-

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