Show simple item record

dc.contributor.authorJayasinghe, K
dc.contributor.authorQuinlan, C
dc.contributor.authorStark, Z
dc.contributor.authorPatel, C
dc.contributor.authorSampson, MG
dc.contributor.authorSaleem, M
dc.contributor.authorMallett, AJ
dc.date.accessioned2020-12-09T23:17:10Z
dc.date.available2020-12-09T23:17:10Z
dc.date.issued2018-01-30
dc.identifierpii: 10.1186/s40246-018-0137-7
dc.identifier.citationJayasinghe, K., Quinlan, C., Stark, Z., Patel, C., Sampson, M. G., Saleem, M. & Mallett, A. J. (2018). Meeting report of the 2017 KidGen Renal Genetics Symposium. HUMAN GENOMICS, 12 (1), https://doi.org/10.1186/s40246-018-0137-7.
dc.identifier.issn1473-9542
dc.identifier.urihttp://hdl.handle.net/11343/253182
dc.description.abstractThe 2017 KidGen Renal Genetics Symposium was held at the Royal Children's Hospital and Murdoch Children's Research Institute, Melbourne, from 6 to 8 December 2017. This meeting addressed clinical, diagnostic, and research aspects of inherited kidney disease. More than 100 clinicians, researchers, and patient representatives attended the conference. The overall goal was to improve the understanding and direction of genomics in renal medicine in Australia and discuss barriers to the use of genomic testing within this area. It also aimed to strengthen collaborations between local, state, and global research and diagnostic and clinical groups.
dc.languageEnglish
dc.publisherBIOMED CENTRAL LTD
dc.titleMeeting report of the 2017 KidGen Renal Genetics Symposium
dc.typeJournal Article
dc.identifier.doi10.1186/s40246-018-0137-7
melbourne.affiliation.departmentPaediatrics (RCH)
melbourne.source.titleHuman Genomics
melbourne.source.volume12
melbourne.source.issue1
dc.rights.licenseCC BY
melbourne.elementsid1305530
melbourne.contributor.authorQuinlan, Catherine
melbourne.contributor.authorStark, Zornitza
dc.identifier.eissn1479-7364
melbourne.accessrightsOpen Access


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record