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

Cunningham, Adam, Fung, Wilson, Massey, Thomas ORCID:, Hall, Jeremy ORCID:, Owen, Michael ORCID:, Van Den Bree, Marianne ORCID: and Peall, Kathryn ORCID: 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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License Start date: 7 May 2020
Item Type: Article
Date Type: Publication
Status: Published
Schools: MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
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

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