Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism-Reference-Cited by-同舟云学术

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Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

Published:2011-10-03 Issue:41 Volume:108 Page:17076-17081
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Horev G.,Ellegood J.,Lerch J. P.,Son Y.-E. E.,Muthuswamy L.,Vogel H.,Krieger A. M.,Buja A.,Henkelman R. M.,Wigler M.,Mills A. A.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference52 articles.

1. Strong Association of De Novo Copy Number Mutations with Autism

2. Genetic variation at the 22q11PRODH2/DGCR6locus presents an unusual pattern and increases susceptibility to schizophrenia

3. Large recurrent microdeletions associated with schizophrenia

4. Rare chromosomal deletions and duplications increase risk of schizophrenia

5. Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability

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