Phenomic determinants of genomic variation in autism spectrum disorders.
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Loss of δ-catenin function in severe autismAbsence of strong strain effects in behavioral analyses of Shank3-deficient miceShould we change targets and methods of early intervention in autism, in favor of a strengths-based education?Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants.Phenotyping, Etiological Factors, and Biomarkers: Toward Precision Medicine in Autism Spectrum Disorders.The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.Pharmacogenomic medicine in autism: challenges and opportunities.Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.Comparison of children with autism spectrum disorder with and without schizophrenia spectrum traits: gender, season of birth, and mental health risk factors.Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.Detection of Genomic Imbalances by Array-Based Comparative Genomic Hybridization in Bulgarian Patients with Autism Spectrum Disorders
P2860
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P2860
Phenomic determinants of genomic variation in autism spectrum disorders.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Phenomic determinants of genomic variation in autism spectrum disorders.
@en
type
label
Phenomic determinants of genomic variation in autism spectrum disorders.
@en
prefLabel
Phenomic determinants of genomic variation in autism spectrum disorders.
@en
P2093
P356
P1476
Phenomic determinants of genomic variation in autism spectrum disorders.
@en
P2093
Chansonette Harvard
J J A Holden
M E S Lewis
M J Hildebrand
N Riendeau
P304
P356
10.1136/JMG.2009.066795
P407
P577
2009-07-21T00:00:00Z