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Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic deletion of approximately 27 genes on chromosome 7, at locus 7q11.23. WS is characterised by an uneven cognitive profile, with serious deficits in visuospatial tasks in comparison to relatively profic...
Autores principales: | Broadbent, Hannah, Farran, Emily K, Chin, Esther, Metcalfe, Kay, Tassabehji, May, Turnpenny, Peter, Sansbury, Francis, Meaburn, Emma, Karmiloff-Smith, Annette |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107613/ https://www.ncbi.nlm.nih.gov/pubmed/25057328 http://dx.doi.org/10.1186/1866-1955-6-18 |
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