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Childhood Predictors of Written Expression in Late Adolescents with 22q11.2 Deletion Syndrome: A Longitudinal Study
BACKGROUND: 22q11.2 Deletion Syndrome (22q11DS) is the second most prevalent genetic syndrome and has a characteristic academic and behavioural phenotype. The primary objective of the current study was to examine the childhood predictors of written expression achievement in adolescents with 22q11DS....
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| Vydáno v: | J Intellect Disabil Res |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5542409/ https://ncbi.nlm.nih.gov/pubmed/28276184 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jir.12370 |
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