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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...
Tallennettuna:
| Julkaisussa: | Am J Med Genet A |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2018
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| Aiheet: | |
| Linkit: | 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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