Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

Meyer-Lindenberg, Andreas, Mervis, Carolyn B., Faith Berman, Karen·2006·Nature Reviews Neuroscience
DOI 10.1038/nrn1906

Cited by (415)

Items 301–400 of 415

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  12. Transposons in the Williams–Beuren Syndrome Critical Region are Associated with Social Behavior in Assistance Dogs
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  14. Notas no percurso: linguagem musical e Síndrome de Williams
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  15. Perfil comunicativo de indivíduos com a síndrome de Williams-Beuren Communicative profile of individuals with Williams-Beuren syndrome
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  16. Stereotypies
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  17. Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.
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  19. Detecção da microdeleção 7q11.23 por MLPA® e estudo clínico dos pacientes com síndrome de Williams-Beuren
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  29. A Del(5 Ncf1 - Fkbp6 ) mouse model of Williams syndrome shows coronary, aortic, and cerebral vascular abnormalities with behavioral deficits
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  38. A long-deletion mouse model of Williams syndrome reveals Ncf1 -dependent modulation of vascular and neural phenotypes
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  44. Numerikus képességek Williams-szindrómában: disszociálódó analóg mennyiségrendszer és verbális előhívás
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  47. Williams Syndrome: The Costs and Benefits of Chromosomal Deletion
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  52. Williams Syndrome-Specific Neuroarchitectural Profile and Its Associations with Cognitive Features
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  54. Characterization of Williams-Beuren Syndrome Mouse Models: Linking Genes with Cognition and Behaviour
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  56. Fenótipo comportamental e cognitivo de crianças e adolescentes com Síndrome de Williams-Beuren****** Behavioral and cognitive phenotype of children and adolescents with Williams-Beuren Syndrome
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