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Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders
BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is a common recurrent neurogenetic condition associated with elevated risk for developmental neuropsychiatric disorders and intellectual disability. Children and adults with 22q11DS often exhibit marked social impairment as well as neurocognitive defic...
Autores principales: | Jalal, Rhideeta, Nair, Aarti, Lin, Amy, Eckfeld, Ariel, Kushan, Leila, Zinberg, Jamie, Karlsgodt, Katherine H., Cannon, Tyrone D., Bearden, Carrie E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052741/ https://www.ncbi.nlm.nih.gov/pubmed/33863277 http://dx.doi.org/10.1186/s11689-021-09363-4 |
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