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Until recently, genetic, neuroanatomical, and psychological
investigations on neurodevelopmental disorders were carried out
independently. Now, tremendous advances across all disciplines have
brought us toward a new scientific frontier: the integration of
molecular genetics with a developmental cognitive neuroscience. The
goal is to understand the basic mechanisms by which genes and
environmental processes contribute to the development of specific
structures and regions of the brain.
This handbook-style volume explores these advances from the
perspective of developmental disorders in children. Research on
children with known genetic disorders offers insights into the genetic
mechanisms that underlie neural development and organization, as
expressed in variations in cognitive profiles. The contributions
provide in-depth analyses of a broad range of neurodevelopmental
disorders, including those resulting from whole chromosome defects
(Down and Turner syndromes), those related to defects in a single gene
(fragile-X syndrome) or a small number of genes (Williams syndrome),
and complex genetic disorders (dyslexia, autism). Contributors from
the fields of teratology and brain injury provide additional
perspectives.
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