1 – 14 of 14
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2012
-
Mark
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2011
-
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
-
Mark
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
(
- Contribution to journal › Article
- 2010
-
Mark
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
(
- Contribution to journal › Article
-
Mark
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
(
- Contribution to journal › Article
- 2009
-
Mark
Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2008
-
Mark
Abnormal melatonin synthesis in autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
Analysis of X chromosome inactivation in autism spectrum disorders
(
- Contribution to journal › Article
- 2007
-
Mark
Mutation screening of the ARX gene in patients with autism
(
- Contribution to journal › Article
-
Mark
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
-
Mark
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
- 2006
-
Mark
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
(
- Contribution to journal › Article