Movement disorder phenotypes in children with 22q11.2 deletion syndrome

Cunningham, Adam, Fung, Wilson, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078

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Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Medicine Neuroscience and Mental Health Research Institute (NMHRI)
Publisher:	Wiley
ISSN:	0885-3185
Funders:	Wellcome Trust, MRC
Date of First Compliant Deposit:	14 April 2020
Date of Acceptance:	6 April 2020
Last Modified:	02 May 2023 19:53
URI:	https://orca.cardiff.ac.uk/id/eprint/130974

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