Works matching IS 18661947 AND DT 2011 AND VI 3 AND IP 2
Results: 8
The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 87, doi. 10.1007/s11689-010-9068-x
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- Article
Association of oxytocin receptor ( OXTR) gene variants with multiple phenotype domains of autism spectrum disorder.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 101, doi. 10.1007/s11689-010-9071-2
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- Article
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 113, doi. 10.1007/s11689-011-9072-9
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- Article
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 124, doi. 10.1007/s11689-011-9076-5
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- Article
Glutathione pathway gene variation and risk of autism spectrum disorders.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 132, doi. 10.1007/s11689-011-9077-4
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- Article
Salivary biomarkers of HPA axis and autonomic activity in adults with intellectual disability with and without stereotyped and self-injurious behavior disorders.
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 144, doi. 10.1007/s11689-011-9080-9
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- Article
Synaptic Wnt signaling-a contributor to major psychiatric disorders?
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- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 162, doi. 10.1007/s11689-011-9083-6
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- Article
Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?
- Published in:
- Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 152, doi. 10.1007/s11689-011-9082-7
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- Article