|
|
Flinders Academic Commons >
Browsing by Author Dimasi, David Paul
Showing results 8 to 13 of 13
| Issue Date | Title | Author(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 |
| 26-Sep-2012 | The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucoma | Wiggs, Janey L; Hewitt, Alex W; Fan, Bao Jian; Wang, Dan Yi; O'Brien, Colm; Realini, Anthony; Craig, Jamie E; Dimasi, David Paul; Mackey, David A; Haines, Jonathan L; Pasquale, Louis R; Figueiredo Sena, Dayse R |
| 2006 | The PITX3 gene in posterior polar congenital
cataract in Australia | Burdon, Kathryn Penelope; McKay, James D; Wirth, M Gabriela; Ruddle, Jonathan; Russell-Eggit, Isabelle M; Bhatti, Samira; Dimasi, David Paul; Mackey, David A; Craig, Jamie E |
| 2007 | Prevalence of CYP1B1 mutations in Australian
patients with primary congenital glaucoma | Elder, James E; Casey, T; Mackey, David A; Craig, Jamie E; MacKinnon, Jane R; Hewitt, Alex W; Dimasi, David Paul; Pater, John Brian; Straga, Tania |
| 2006 | The role of the Met98Lys optineurin variant in
inherited optic nerve diseases | Craig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A |
| 2004 | RZF, a zinc-finger protein in the photoreceptors
of human retina | Higginson, K A; Sharma, Shiwani; Della, N G; Dimasi, David Paul |
Showing results 8 to 13 of 13
|
