Deep phenotyping of speech and language skills in 16p11.2 deletion syndrome
Mei, C., Fedorenko, E., Amor, D., Boys, A., Hoeflin, C., Carew, P., Burgess, T., Fisher, S. & Morgan, A. 2018. European Journal of Human Genetics, 26(5), 676-686. DOI: 10.1038/s41431-018-0102-x. PMID: 29445122. PMC5945616.
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A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
Fedorenko, E.*, Morgan, A.*, Murray, E., Cardinaux, A., Mei, C., Tager-Flusberg, H., Fisher, S. & Kanwisher, N. 2016. European Journal of Human Genetics, 24(2), 302-306. DOI: 10.1038/ejhg.2015.149. PMID: 26763793. PMC4717201.
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