Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/16724
Title: Blake's pouch cyst in 13q deletion syndrome: posterior fossa malformations may occur due to disruption of multiple genes
Authors: Myers, Kenneth A;Wallis, Mathew J;Fitt, Gregory J;Sarnat, Harvey B;Newton, Mark R
Affiliation: Department of Radiology, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Department of Neurology, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Department of Clinical Genetics, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Department of Paediatrics, Section of Neurology, University of Calgary Cumming School of Medicine, Alberta Children's Hospital, Calgary, Alberta, Canada
Issue Date: Sep-2017
EDate: 2017-07-07
Citation: American Journal of Medical Genetics 2017; 173(9): 2442-2445
Description: Research letter
URI: http://ahro.austin.org.au/austinjspui/handle/1/16724
DOI: 10.1002/ajmg.a.38346
ORCID: 0000-0001-7831-4593
PubMed URL: https://www.ncbi.nlm.nih.gov/pubmed/28686337
Type: Journal Article
Appears in Collections:Journal articles

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