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https://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 | Austin 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 | Date: | 2017-07-07 | Publication information: | American Journal of Medical Genetics 2017; 173(9): 2442-2445 | Description: | Research letter | URI: | https://ahro.austin.org.au/austinjspui/handle/1/16724 | DOI: | 10.1002/ajmg.a.38346 | ORCID: | 0000-0001-7831-4593 | Journal: | American Journal of Medical Genetics | PubMed URL: | https://pubmed.ncbi.nlm.nih.gov/28686337 | Type: | Journal Article |
| Appears in Collections: | Journal articles |
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