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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...

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Dades bibliogràfiques
Publicat a:J Neurodev Disord
Autors principals: Jalal, Rhideeta, Nair, Aarti, Lin, Amy, Eckfeld, Ariel, Kushan, Leila, Zinberg, Jamie, Karlsgodt, Katherine H., Cannon, Tyrone D., Bearden, Carrie E.
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2021
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8052741/
https://ncbi.nlm.nih.gov/pubmed/33863277
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-021-09363-4
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