Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/62707
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dc.contributor.authorCorbett, M.en
dc.contributor.authorGecz, J.en
dc.date.issued2010en
dc.identifier.citationExpert Review of Molecular Diagnostics, 2010; 10(7):833-836en
dc.identifier.issn1473-7159en
dc.identifier.issn1744-8352en
dc.identifier.urihttp://hdl.handle.net/2440/62707-
dc.description.statementofresponsibilityMark Corbett, Jozef Geczen
dc.language.isoenen
dc.publisherFuture Drugs Ltd.en
dc.rights© 2010 Expert Reviews Ltd.en
dc.subjectdeep resequencing; genomics; Indel; next-generation sequencing; sequence capture; SNP; variation; X-linkeden
dc.titleGreat expectations: using massively parallel sequencing to solve inherited disordersen
dc.typeJournal articleen
dc.identifier.rmid0020101557en
dc.identifier.doi10.1586/ERM.10.83en
dc.identifier.pubid32897-
pubs.library.collectionGenetics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidCorbett, M. [0000-0001-9298-3072]en
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Genetics publications

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