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PreviewIssue DateTitleAuthor(s)
2010Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness PublicationMartin, Nicholas G; Young, Terri L; Hammond, Christopher J; Li, Yi JU; Mitchell, P; Healey, Paul R; Montgomery, G W; Hansell, Narelle; Spector, Tim D; Macgregor, Stuart; Craig, Jamie; Mackey, David A; Lu, Y; Dimasi, David Paul; Hysi, Pirro G; Hewitt, Alex W; Burdon, Kathryn Penelope; Toh, Tze'Yo; Ruddle, Jonathan
Feb-2013Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconusLu, Y; Vitart, V; Burdon, Kathryn P; Khor, CC
2004Human PXR variants and their differential effects on the regulation of human UDP-glucuronosyltransferase gene expressionXie, W; Mackenzie, Peter Ian; Gardner-Stephen, Dione Anne; Radominska-Pandya, A; Goyal, A; Heydel, J M; Lindblom, T; Lu, Y
Showing results 1 to 3 of 3

 

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