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Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion
Recurrent deletions of a ~600-kb region of 16p11.2 have been associated with a highly penetrant form of childhood apraxia of speech (CAS). Yet prior findings have been based on a small, potentially biased sample using retrospectively collected data. We examine the prevalence of CAS in a larger cohor...
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| Publicado en: | Eur J Hum Genet |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer International Publishing
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5945616/ https://ncbi.nlm.nih.gov/pubmed/29445122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0102-x |
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