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Flinders Academic Commons >
Browsing by Author Chen, Celia S
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) | | 2003 | Hereditary hyperferritinemia-cataract syndrome:
prevalence, lens morphology, spectrum of mutations, and clinical presentations | Toohey, 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 |
| 2009 | Multiple sclerosis presenting with homonymous hemianopia | Law, Siew W; Lee, Andrew W; Chen, Celia S |
| 2007 | A novel deletion in the FTL gene causes hereditary
hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start
site | Burdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S |
| 2009 | Optic neuritis - more than a loss of vision | Chu, Edward R; Chen, Celia S |
Showing results 1 to 4 of 4
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