Freeth, M. orcid.org/0000-0003-0534-9095, Al-Jawahiri, R. orcid.org/0000-0002-5689-3368, Smith, H. et al. (1 more author) (2021) Speech, language and communication phenotyping in rare genetic syndromes: Commentary on Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics, 29 (8). pp. 1166-1167. ISSN 1018-4813
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2021 The Author(s), under exclusive licence to European Society of Human Genetics. This is an author-produced version of a paper subsequently published in European Journal of Human Genetics. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Science (Sheffield) > Department of Psychology (Sheffield) |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 22 Sep 2021 11:11 |
Last Modified: | 20 Feb 2022 01:38 |
Status: | Published |
Publisher: | Springer Science and Business Media LLC |
Refereed: | Yes |
Identification Number: | 10.1038/s41431-021-00942-6 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:178419 |