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Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome
The chromosome 1q21.1 duplication syndrome (OMIM# 612475) is characterized by head anomalies, mild facial dysmorphisms, and cognitive problems, including autistic features, mental retardation, developmental delay, and learning disabilities. Speech and language development are sometimes impaired, but...
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| Publié dans: | Front Pediatr |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Frontiers Media S.A.
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5996825/ https://ncbi.nlm.nih.gov/pubmed/29922639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2018.00163 |
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