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Neurodevelopmental outcome in 22q11.2 deletion syndrome and management

The 22q11.2 deletion syndrome (22q11.2 DS) places affected individuals at an increased risk for neurodevelopmental/cognitive, behavioral and social–emotional difficulties. Poor cognitive functioning and intellectual disabilities, attention and executive functioning deficits, learning disorders, emot...

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Detalhes bibliográficos
Publicado no:Am J Med Genet A
Main Authors: Swillen, Ann, Moss, Edward, Duijff, Sasja
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6202262/
https://ncbi.nlm.nih.gov/pubmed/29696780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38709
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