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Morison, L, Meffert, E, Stampfer, M, Steiner-Wilke, I, Vollmer, B, Schulze, K, Briggs, T, Braden, R, Vogel, AP, Thompson-Lake, D, et al. Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
2022
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St John, M, Amor, DJ, Morgan, AT. Speech and language development and genotype–phenotype correlation in 49 individuals with KAT6A syndrome.
American Journal of Medical Genetics Part A
188(12)
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3389 -3400
2022
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Gasparini, L, Shepherd, D, Bavin, EL, Eadie, P, Reilly, S, Morgan, A, Wake, M. Using machine-learning methods to identify early-life predictors of 11-year language outcome.
2022
view publication
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John, MS, Reyk, OV, Koolen, D, de Vries, B, Amor, D, Morgan, A. Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature.
2022
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Mountford, H, Braden, R, Morgan, A, Newbury, D. Genetic Studies of Language Disorders.
45 -77
2022
view publication