Works matching IS 18661947 AND DT 2011 AND VI 3 AND IP 1
Results: 9
Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 3, doi. 10.1007/s11689-010-9059-y
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Electrophysiological study of local/global processing in Williams syndrome.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 28, doi. 10.1007/s11689-010-9064-1
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Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 39, doi. 10.1007/s11689-010-9065-0
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Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 57, doi. 10.1007/s11689-010-9067-y
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Angelman syndrome: advancing the research frontier of neurodevelopmental disorders.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 50, doi. 10.1007/s11689-010-9066-z
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- Article
How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 68, doi. 10.1007/s11689-010-9069-9
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- Article
Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 76, doi. 10.1007/s11689-010-9070-3
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List of reviewers for 2010.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 2, doi. 10.1007/s11689-011-9073-8
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- Article
Cover art description.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 1, p. 1, doi. 10.1007/s11689-011-9075-6
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- Article