Autistic behavior in boys with fragile X syndrome: social approach and HPA-axis dysfunction.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 283, doi. 10.1007/s11689-009-9028-5
- By:
- Publication type:
- Article
Works matching IS 18661947 AND DT 2009 AND VI 1 AND IP 4
Results: 7
1
2
Deficient NRG1-ERBB signaling alters social approach: relevance to genetic mouse models of schizophrenia.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 302, doi. 10.1007/s11689-009-9017-8
- By:
- Publication type:
- Article
3
Novel copy number variants in children with autism and additional developmental anomalies.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 292, doi. 10.1007/s11689-009-9013-z
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- Publication type:
- Article
4
Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 264, doi. 10.1007/s11689-009-9031-x
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- Publication type:
- Article
5
Choline transporter gene variation is associated with attention-deficit hyperactivity disorder.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 252, doi. 10.1007/s11689-009-9033-8
- By:
- Publication type:
- Article
6
Variable phenotypic expression of a MECP2 mutation in a family.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 313, doi. 10.1007/s11689-009-9034-7
- By:
- Publication type:
- Article
7
Cover essay.
- Published in:
- Journal of Neurodevelopmental Disorders, 2009, v. 1, n. 4, p. 251, doi. 10.1007/s11689-009-9038-3
- Publication type:
- Article