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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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| Publicat a: | J Neurodev Disord |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| 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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