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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License URL: http://creativecommons.org/licenses/by/4.0
License Start date: 7 May 2020
Official URL: http://dx.doi.org/10.1002/mds.28078
| Item Type: | Article |
|---|---|
| Date Type: | Publication |
| Status: | Published |
| Schools: | Research Institutes & Centres > MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Schools > Medicine Research Institutes & Centres > Neuroscience and Mental Health Research Institute (NMHII) |
| 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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