Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes

BACKGROUND: Chromosome 22q11.2 deletion syndrome (22q11.2DS), fragile X syndrome (FXS), and Turner syndrome (TS) are complex and variable developmental syndromes caused by different genetic abnormalities; yet, they share similar cognitive impairments in the domains of numbers, space, and time. The a...

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Detalles Bibliográficos
Autores principales: Quintero, Andrea I, Beaton, Elliott A, Harvey, Danielle J, Ross, Judith L, Simon, Tony J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995552/
https://www.ncbi.nlm.nih.gov/pubmed/24628892
http://dx.doi.org/10.1186/1866-1955-6-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995552/
https://www.ncbi.nlm.nih.gov/pubmed/24628892
http://dx.doi.org/10.1186/1866-1955-6-5

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