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Genomic and epigenetic evidence for oxytocin receptor deficiency in autismHyperbaric treatment for children with autism: a multicenter, randomized, double-blind, controlled trialAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisAutism spectrum disorders: is mesenchymal stem cell personalized therapy the future?Autism spectrum disordersAutism and Metabolic DiseasesAntipsychotics in the treatment of autismAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistGenetics evaluation for the etiologic diagnosis of autism spectrum disordersMinor physical anomalies in autism: a meta-analysisPrenatal stress and risk for autismConvulsing toward the pathophysiology of autismAutism as a Natural Human Variation: Reflections on the Claims of the Neurodiversity MovementHyperbaric oxygen therapy for autism spectrum disorder (ASD) in children and adultsAcupuncture for autism spectrum disorders (ASD)Acupuncture for autistic spectrum disorderA comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromesIdentification of significant association and gene-gene interaction of GABA receptor subunit genes in autismLinkage and candidate gene studies of autism spectrum disorders in European populationsEndocrine disruptors and childhood social impairmentAutism risk factors: genes, environment, and gene-environment interactionsRare structural variation of synapse and neurotransmission genes in autismWhat can we learn about autism from studying fragile X syndrome?dbCRID: a database of chromosomal rearrangements in human diseasesShared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorderMitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisBehavioral and cerebellar transmission deficits in mice lacking the autism-linked gene islet brain-2Molecular and cognitive predictors of the continuum of autistic behaviours in fragile XA genetic variant that disrupts MET transcription is associated with autismAutistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersGenome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlatesDoes Rubella Cause Autism: A 2015 Reappraisal?Urinary Biomarkers of Brain DiseasesFrom Autism to Eating Disorders and More: The Role of Oxytocin in Neuropsychiatric DisordersPlacental Barrier and Autism Spectrum Disorders: The Role of Prolactin and Dopamine on the Developing Fetal BrainThe Impact of Neuroimmune Alterations in Autism Spectrum DisorderExcitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum DisordersGenomics and autism spectrum disorderFunctional magnetic resonance imaging in awake transgenic fragile X rats: evidence of dysregulation in reward processing in the mesolimbic/habenular neural circuit
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
The genetics of autism
@ast
The genetics of autism
@en
The genetics of autism
@nl
type
label
The genetics of autism
@ast
The genetics of autism
@en
The genetics of autism
@nl
prefLabel
The genetics of autism
@ast
The genetics of autism
@en
The genetics of autism
@nl
P2093
P3181
P356
P1433
P1476
The genetics of autism
@en
P2093
Isabelle Rapin
Rebecca Muhle
Stephanie V Trentacoste
P304
P3181
P356
10.1542/PEDS.113.5.E472
P407
P577
2004-05-01T00:00:00Z