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- 2011
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Mark
Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
(
- Contribution to journal › Article
- 2010
-
Mark
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
(
- Contribution to journal › Article
- 2009
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Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
(
- Contribution to journal › Article
- 2008
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Mark
Abnormal melatonin synthesis in autism spectrum disorders
(
- Contribution to journal › Article
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Mark
Analysis of X chromosome inactivation in autism spectrum disorders
(
- Contribution to journal › Article
- 2005
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Mark
Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
(
- Contribution to journal › Article
- 2003
-
Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article