Identification and molecular characterization of two novel chromosomal deletions associated with autism.
about
A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Autism-associated gene Dlgap2 mutant mice demonstrate exacerbated aggressive behaviors and orbitofrontal cortex deficitsChromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese populationResequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese PopulationGenotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome.Copy number variations in Saudi family with intellectual disability and epilepsy.Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disordersRole of the DLGAP2 gene encoding the SAP90/PSD-95-associated protein 2 in schizophrenia.Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.MASL1: a neglected ROCO protein.High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.Isolated chromosome 8p23.2‑pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders.12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.Chromosomal abnormalities in patients with autism spectrum disorders from Taiwan.Impairment of social behaviors in Arhgef10 knockout mice.Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.Response to Nucaro et al
P2860
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P2860
Identification and molecular characterization of two novel chromosomal deletions associated with autism.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Identification and molecular c ...... etions associated with autism.
@en
Identification and molecular c ...... etions associated with autism.
@nl
type
label
Identification and molecular c ...... etions associated with autism.
@en
Identification and molecular c ...... etions associated with autism.
@nl
prefLabel
Identification and molecular c ...... etions associated with autism.
@en
Identification and molecular c ...... etions associated with autism.
@nl
P2093
P2860
P1433
P1476
Identification and molecular c ...... etions associated with autism.
@en
P2093
P2860
P304
P356
10.1111/J.1399-0004.2010.01395.X
P577
2010-11-01T00:00:00Z