Identifying neurocognitive phenotypes in autism
Author:
Affiliation:
1. Laboratory of Developmental Cognitive Neuroscience, Department of Anatomy and Neurobiology, Boston University School of Medicine, 715 Albany Street L-814, Boston, MA 02118, USA
Abstract
Publisher
The Royal Society
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Link
https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.2002.1198
Reference108 articles.
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2. Amir R. Van den Veyver I. Wan M. Tran C. Francke U. & Zoghbi H. 1999 Rett syndrome is caused by mutations in X-linked MECP2 encoding methyl-CpG-binding protein
3. Nature Genet. 23 185-188.
4. Autism as a strongly genetic disorder: evidence from a British twin study
5. Autism: Towards an Integration of Clinical, Genetic, Neuropsychological, and Neurobiological Perspectives
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