Functional outcomes of adults with 22q11.2 deletion syndrome | Zendy

Nancy J. Butcher | Zendy; Eva W.C. Chow | Zendy; Gregory Costain | Zendy; Dominique J. Karas | Zendy; Andrew Fu Wah Ho | Zendy; Anne S. Bassett | Zendy

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Functional outcomes of adults with 22q11.2 deletion syndrome

Author(s) -

Nancy J. Butcher,

Eva W.C. Chow,

Gregory Costain,

Dominique J. Karas,

Andrew Fu Wah Ho,

Anne S. Bassett

Publication year - 2012

Publication title -

genetics in medicine

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.509

H-Index - 128

eISSN - 1530-0366

pISSN - 1098-3600

DOI - 10.1038/gim.2012.66

Subject(s) - vineland adaptive behavior scale , intellectual disability , activities of daily living , mood , affect (linguistics) , intelligence quotient , anxiety , schizophrenia (object oriented programming) , deletion syndrome , psychology , clinical psychology , medicine , psychiatry , cognition , phenotype , genetics , communication , biology , gene

The 22q11.2 deletion syndrome is a common multisystem genomic disorder with congenital and later-onset manifestations, including congenital heart disease, intellectual disability, and psychiatric illness, that may affect long-term functioning. There are limited data on adult functioning in 22q11.2 deletion syndrome.

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