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dc.contributor.authorDickinson, Joanne L
dc.contributor.authorSale, Michele M
dc.contributor.authorPassmore, Abraham
dc.contributor.authorFitzgerald, Liesel M
dc.contributor.authorWheatley, Catherine M
dc.contributor.authorBurdon, Kathryn Penelope
dc.contributor.authorCraig, Jamie E
dc.contributor.authorTengtrisorn, Supaporn
dc.contributor.authorCarden, Susan M
dc.contributor.authorMaclean, Hector
dc.contributor.authorMackey, David A
dc.date.accessioned2010-07-27T06:20:11Z
dc.date.available2010-07-27T06:20:11Z
dc.date.issued2006en_US
dc.identifier.citationDickinson, J.L., Sale, M.M., Passmore, A., Fitzgerald, L.M., Wheatley, C.M., Burdon, K.P., Craig, J., Tengtrisorn, S., Carden, S.M., Maclean, H., et al., 2006. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. Clinical and Experimental Ophthalmology, 34(7), 682-688.en
dc.identifier.issn1442-6404en_US
dc.identifier.urihttp://hdl.handle.net/2328/11220
dc.titleMutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurityen_US
dc.typeArticleen_US
dc.identifier.rmid2006003740en_US
dc.identifier.doihttps://doi.org/10.1111/j.1442-9071.2006.01314.xen
dc.subject.forgroup1113 Ophthalmology and Optometryen_US
dc.subject.forgroup1103 Clinical Sciencesen_US
dc.subject.forgroup1117 Public Health and Health Servicesen_US


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