Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nrn1906.pdf
Reference171 articles.
1. Strømme, P., Bjørnstad, P. G. & Ramstad, K. Prevalence estimation of Williams syndrome. J. Child Neurol. 17, 269–271 (2002).
2. Beuren, A. J., Apitz, J. & Harmjanz, D. Supravalvular aortic stenosis in association with mental retardation and a certain facial appearance. Circulation 26, 1235–1240 (1962).
3. Williams, J. C., Barratt-Boyes, B. G. & Lowe, J. B. Supravalvular aortic stenosis. Circulation 24, 1311–1318 (1961). The initial description of WS.
4. American Academy of Pediatrics: Health care supervision for children with Williams syndrome. Pediatrics 107, 1192–1204 (2001).
5. Morris, C. A. et al. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype–phenotype analysis of five families with deletions in the Williams syndrome region. Am. J. Med. Genet. 123A, 45–59 (2003). Provides evidence that GTF2I is important for normal intellectual ability.
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