Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
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Rare deletions at the neurexin 3 locus in autism spectrum disorderDeveloping Medications Targeting Glutamatergic Dysfunction in Autism: Progress to DateFusion of large-scale genomic knowledge and frequency data computationally prioritizes variants in epilepsySynaptic proteins and receptors defects in autism spectrum disordersAbsence of strong strain effects in behavioral analyses of Shank3-deficient miceA genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network.De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention ProblemsIntegrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder.AKAPs integrate genetic findings for autism spectrum disorders.Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disordersGenome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.Genetic architecture of reciprocal CNVs.SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.Glutamatergic candidate genes in autism spectrum disorder: an overview.Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes.Phelan McDermid Syndrome: From Genetic Discoveries to Animal Models and Treatment.Rare copy number variants are common in young children with autism spectrum disorder.Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity.Heritable genotype contrast mining reveals novel gene associations specific to autism subgroups.Inference of Causative Genes for Alzheimer's Disease Due to Dosage Imbalance.Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.Molecular Karyotyping in Children and Adolescents with Gender DysphoriaAssociation of Copy Number Variations in Autism Spectrum Disorders: A Systematic Review
P2860
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P2860
Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
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name
Copy number variation characte ...... ith autism spectrum disorders.
@en
Copy number variation characte ...... ith autism spectrum disorders.
@nl
type
label
Copy number variation characte ...... ith autism spectrum disorders.
@en
Copy number variation characte ...... ith autism spectrum disorders.
@nl
prefLabel
Copy number variation characte ...... ith autism spectrum disorders.
@en
Copy number variation characte ...... ith autism spectrum disorders.
@nl
P2093
P2860
P50
P356
P1476
Copy number variation characte ...... ith autism spectrum disorders.
@en
P2093
Anna Bremer
Asa Uppströmer
Britt-Marie Anderlid
Elisabeth Fernell
Jacqueline Schoumans
MaiBritt Giacobini
Peter Gustavsson
Viviann Nordin
P2860
P304
P356
10.1002/AJMG.B.31142
P577
2010-12-08T00:00:00Z