Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11970
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dc.contributor.authorBerkovic, Samuel Fen
dc.contributor.authorGecz, Jozefen
dc.date.accessioned2015-05-16T01:36:18Z-
dc.date.available2015-05-16T01:36:18Z-
dc.date.issued2013-11-29en
dc.identifier.citationThe Lancet. Neurology 2013; 13(1): 24-5en
dc.identifier.govdoc24291219en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/11970en
dc.language.isoenen
dc.subject.otherCarrier Proteins.geneticsen
dc.subject.otherCraniofacial Abnormalities.geneticsen
dc.subject.otherExome.geneticsen
dc.subject.otherFemaleen
dc.subject.otherHand Deformities, Congenital.geneticsen
dc.subject.otherHearing Loss, Sensorineural.geneticsen
dc.subject.otherHumansen
dc.subject.otherIntellectual Disability.geneticsen
dc.subject.otherInternationalityen
dc.subject.otherMaleen
dc.subject.otherNails, Malformed.geneticsen
dc.subject.otherPhenotypeen
dc.subject.otherSequence Analysis, DNA.methodsen
dc.titlePhenotype-genotype complexities: opening DOORS.en
dc.typeJournal Articleen
dc.identifier.journaltitleThe Lancet. Neurologyen
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSchool of Paediatrics and Reproductive Health, The University of Adelaide at the Women's and Children's Hospital, North Adelaide, Adelaide SA 5006, Australiaen
dc.identifier.doi10.1016/S1474-4422(13)70237-0en
dc.description.pages24-5en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24291219en
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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