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Browsing by Author Hewitt, Alex W

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PreviewIssue DateTitleAuthor(s)
2009Rapid inexpensive genome-wide association using pooled whole bloodCraig, Jamie; Sharma, Shiwani; Hewitt, Alex W; McMellon, Amy E; Henders, Anjali K; Wallace, Leanne; Ma, Lingjun; Burdon, Kathryn Penelope; Visscher, Peter; Montgomery, Grant; Macgregor, Stuart
2006The role of the Met98Lys optineurin variant in inherited optic nerve diseasesCraig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A
2009Sensitivity of confocal laser tomography versus optical coherence tomography in detecting advanced glaucomaHewitt, Alex W; Straga, Tania; Landers, John A; Chappell, Angela J.; Mills, Richard Arthur; Craig, Jamie
2009A systematic meta-analysis of genetic association studies for diabetic retinopathyAbhary, Sotoodeh; Hewitt, Alex W; Craig, Jamie; Burdon, Kathryn Penelope
2010Systemic disease association of familial and sporadic glaucome: the glaucoma inheritance study inTasmaniaLai, Tze; Green, Catherine M; Wu, Johnny; Mackey, David A; Kearns, Lisa A; Craig, Jamie; Hewitt, Alex W
2010Tag SNPs detect association of teh CYP1B1 gene with primary open angle glaucomaBurdon, Kathryn Penelope; Hewitt, Alex W; Mackey, David A; Craig, Jamie; Mitchell, Paul
Jul-2005The 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
2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesMcKay, 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
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