Speech, language and communication phenotyping in rare genetic syndromes: Commentary on Speech and language deficits are central to SETBP1 haploinsufficiency disorder

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

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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:
  • Published (online): 20 August 2021
  • Published: August 2021
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: https://doi.org/10.1038/s41431-021-00942-6
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