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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/107068
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dc.contributor.authorEllingford, J.-
dc.contributor.authorBarton, S.-
dc.contributor.authorBhaskar, S.-
dc.contributor.authorWilliams, S.-
dc.contributor.authorSergouniotis, P.-
dc.contributor.authorO'Sullivan, J.-
dc.contributor.authorLamb, J.-
dc.contributor.authorPerveen, R.-
dc.contributor.authorHall, G.-
dc.contributor.authorNewman, W.-
dc.contributor.authorBishop, P.-
dc.contributor.authorRoberts, S.-
dc.contributor.authorLeach, R.-
dc.contributor.authorTearle, R.-
dc.contributor.authorBayliss, S.-
dc.contributor.authorRamsden, S.-
dc.contributor.authorNemeth, A.-
dc.contributor.authorBlack, G.-
dc.date.issued2016-
dc.identifier.citationOphthalmology, 2016; 123(5):1143-1150-
dc.identifier.issn0161-6420-
dc.identifier.issn1549-4713-
dc.identifier.urihttp://hdl.handle.net/2440/107068-
dc.description.abstractAbstract not available-
dc.description.statementofresponsibilityJamie M. Ellingford, Stephanie Barton, Sanjeev Bhaskar, Simon G. Williams, Panagiotis I. Sergouniotis, James O, Sullivan, Janine A. Lamb, Rahat Perveen, Georgina Hall, William G. Newman, Paul N. Bishop, Stephen A. Roberts, Rick Leach, Rick Tearle, Stuart Bayliss, Simon C. Ramsden, Andrea H. Nemeth, Graeme C.M. Black-
dc.language.isoen-
dc.publisherAmerican Academy of Ophthalmology-
dc.rights© 2016 by the American Academy of Ophthalmology. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).-
dc.source.urihttp://dx.doi.org/10.1016/j.ophtha.2016.01.009-
dc.subjectHumans-
dc.subjectEye Diseases, Hereditary-
dc.subjectRetinal Diseases-
dc.subjectMolecular Diagnostic Techniques-
dc.subjectSensitivity and Specificity-
dc.subjectRetrospective Studies-
dc.subjectSequence Analysis, DNA-
dc.subjectGenotype-
dc.subjectPolymorphism, Single Nucleotide-
dc.subjectGenome-
dc.subjectFemale-
dc.subjectMale-
dc.subjectHigh-Throughput Nucleotide Sequencing-
dc.titleWhole genome sequencing increases molecular diagnostic yield compared with current diagnostic testing for inherited retinal disease-
dc.typeJournal article-
dc.identifier.doi10.1016/j.ophtha.2016.01.009-
pubs.publication-statusPublished-
dc.identifier.orcidTearle, R. [0000-0003-2243-5091]-
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Opthalmology & Visual Sciences publications

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