Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16724
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dc.contributor.authorMyers, Kenneth A-
dc.contributor.authorWallis, Mathew J-
dc.contributor.authorFitt, Gregory J-
dc.contributor.authorSarnat, Harvey B-
dc.contributor.authorNewton, Mark R-
dc.date2017-07-07-
dc.date.accessioned2017-07-26T00:49:20Z-
dc.date.available2017-07-26T00:49:20Z-
dc.date.issued2017-09-
dc.identifier.citationAmerican Journal of Medical Genetics 2017; 173(9): 2442-2445en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16724-
dc.descriptionResearch letteren_US
dc.titleBlake's pouch cyst in 13q deletion syndrome: posterior fossa malformations may occur due to disruption of multiple genesen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAmerican Journal of Medical Geneticsen_US
dc.identifier.affiliationDepartment of Radiology, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Neurology, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Clinical Genetics, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Paediatrics, Section of Neurology, University of Calgary Cumming School of Medicine, Alberta Children's Hospital, Calgary, Alberta, Canada-
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28686337en_US
dc.identifier.doi10.1002/ajmg.a.38346en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-7831-4593-
dc.type.austinJournal Articleen_US
local.name.researcherFitt, Gregory J
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptClinical Genetics-
crisitem.author.deptRadiology-
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