Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 161, Issue 4, Pages 845-849
Publisher
Wiley
Online
2013-02-27
DOI
10.1002/ajmg.a.35754
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The 3q29 microdeletion syndrome: Report of three new unrelated patients and in silico “RNA binding” analysis of the 3q29 region
- (2011) Majed J. Dasouki et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia
- (2011) L.S. Carroll et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
- (2011) Erin B. Kaminsky et al. GENETICS IN MEDICINE
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
- (2010) Fabiola Quintero-Rivera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder
- (2010) Jill Clayton-Smith et al. CLINICAL DYSMORPHOLOGY
- 1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child
- (2010) William Cobb et al. European Journal of Medical Genetics
- The role of SAP97 in synaptic glutamate receptor dynamics
- (2010) MacKenzie A. Howard et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Fbxo45, a Novel Ubiquitin Ligase, Regulates Synaptic Activity
- (2009) Hirobumi Tada et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Fbxo45 Forms a Novel Ubiquitin Ligase Complex and Is Required for Neuronal Development
- (2009) T. Saiga et al. MOLECULAR AND CELLULAR BIOLOGY
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Metabotropic glutamate receptor type 5 in levodopa-induced motor complications
- (2009) Bazoumana Ouattara et al. NEUROBIOLOGY OF AGING
- Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited
- (2008) Judith Rapoport et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Copy-number variations associated with neuropsychiatric conditions
- (2008) Edwin H. Cook Jr et al. NATURE
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
- (2008) Blake C Ballif et al. Molecular Cytogenetics
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now