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Title
Genotype to phenotype relationships in autism spectrum disorders
Authors
Keywords
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Journal
NATURE NEUROSCIENCE
Volume 18, Issue 2, Pages 191-198
Publisher
Springer Nature
Online
2014-12-23
DOI
10.1038/nn.3907
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- (2013) Gordon M. G. Shepherd NATURE REVIEWS NEUROSCIENCE
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- (2012) Manuel Ascano et al. NATURE
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- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
- Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities
- (2012) H. Y. Zoghbi et al. Cold Spring Harbor Perspectives in Biology
- Autism genetics: searching for specificity and convergence
- (2012) Jamee M Berg et al. GENOME BIOLOGY
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- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
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- Genetics of autism spectrum disorders
- (2011) Daniel H. Geschwind TRENDS IN COGNITIVE SCIENCES
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- Genetic Heterogeneity in Human Disease
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- Epidemiology of Pervasive Developmental Disorders
- (2009) Eric Fombonne PEDIATRIC RESEARCH
- The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
- (2009) Catalina Betancur et al. TRENDS IN NEUROSCIENCES
- The Autistic Neuron: Troubled Translation?
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- Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types
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- (2008) I. Feldman et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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