Speech and language classification in the human phenotype ontology
Author:
Funder
Department of Health | National Health and Medical Research Council
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41431-024-01635-6.pdf
Reference9 articles.
1. Liégeois FJ, Turner SJ, Mayes A, Bonthrone AF, Boys A, Smith L, et al. Dorsal language stream anomalies in an inherited speech disorder. Brain. 2019;142:966–77.
2. Liégeois FJ, Hildebrand MS, Bonthrone A, Turner SJ, Scheffer IE, Bahlo M, et al. Early neuroimaging markers of FOXP2 intragenic deletion. Sci Rep. 2016;6:35192.
3. Thompson-Lake DGY, Scerri TS, Block S, Turner SJ, Reilly S, Kefalianos E, et al. Atypical development of Broca’s area in a large family with inherited stuttering. Brain. 2022;145:1177–88.
4. Morgan AT, Scerri TS, Vogel AP, Reid CA, Quach M, Jackson VE, et al. Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain. 2023;146:5086–97.
5. Morison LD, Meffert E, Stampfer M, Steiner-Wilke I, Vollmer B, Schulze K, et al. In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. J Med Genet. 2023;60:597–607.
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