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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Bibliographische Detailangaben
Veröffentlicht in:Front Pediatr
Hauptverfasser: Benítez-Burraco, Antonio, Barcos-Martínez, Montserrat, Espejo-Portero, Isabel, Fernández-Urquiza, Maite, Torres-Ruiz, Raúl, Rodríguez-Perales, Sandra, Jiménez-Romero, Ma Salud
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2018
Schlagworte:
Pediatrics
Online Zugang: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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