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Flinders Academic Commons >
Browsing by Author Hewitt, Alex W
Showing results 14 to 22 of 22
| Preview | Issue Date | Title | Author(s) | | 2008 | Myocilin allele-specific glaucoma phenotype
database | Craig, Jamie E; Hewitt, Alex W; Mackey, David A |
| 2006 | A myocilin Gln368STOP homozygote does not exhibit
a more severe glaucoma phenotype than heterozygous cases | Hewitt, Alex W; Bennett, Sonya L; Dimasi, David Paul; Craig, Jamie E; Mackey, David A |
| 2007 | Myocilin Gly252Arg mutation and glaucoma of
intermediate severity in caucasian individuals | Hewitt, Alex W; Bennett, Sonya L; Richards, J E; Dimasi, David Paul; Booth, Adam P; Inglehearn, Chris; Anwar, Rashida; Yamamoto, Tetsuya; Fingert, John H; Heon, Elise; Craig, Jamie E; Mackey, David A |
| 2007 | The optic nerve head in myocilin
glaucoma | Hewitt, Alex W; Bennett, Sonya L; Fingert, John H; Cooper, Richard L; Stone, Edwin M; Craig, Jamie E; Mackey, David A |
| 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 |
| 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 |
| Jul-2005 | The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. | McKay, James D; Patterson, B; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Hewitt, Alex W; Cohn, Amy C; Kerdraon, Y; Mackey, David A |
| 2005 | The telomere of human chromosome 1p contains at
least two independent autosomal dominant congenital cataract genes | McKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W |
Showing results 14 to 22 of 22
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