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

Cunningham, Adam, Fung, Wilson, Massey, Thomas, Hall, Jeremy, Owen, Michael, Van Den Bree, Marianne and Peall, Kathryn 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 10.1002/mds.28078

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Item Type: Article
Date Type: Published Online
Status: In Press
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: 30 Jun 2020 14:38
URI: http://orca.cf.ac.uk/id/eprint/130974

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