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Browsing by Author Chen, Celia S

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PreviewIssue DateTitleAuthor(s)
2003Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentationsToohey, M G; Chen, Celia S; Craig, Jamie E; Mackey, David A; Wirth, M Gabriela; Clark, J B; Elder, James E; Grant, G; McLeod, J L; Kirkland, M A; Kowal, L; Roberts, S; Savoia, H F
2009Multiple sclerosis presenting with homonymous hemianopiaLaw, Siew W; Lee, Andrew W; Chen, Celia S
2007A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteBurdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S
2009Optic neuritis - more than a loss of visionChu, Edward R; Chen, Celia S
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