about
HERVs expression in Autism Spectrum DisordersAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisAdvances in autism genetics: on the threshold of a new neurobiologyThe role of immune dysfunction in the pathophysiology of autismLoss of δ-catenin function in severe autismHeterogeneity and the genetics of autism.A genomic screen of autism: evidence for a multilocus etiology.Autism risk factors: genes, environment, and gene-environment interactionsNeurexins and neuroligins: recent insights from invertebratesMultiple rare variants in the etiology of autism spectrum disordersAutism or atypical autism in maternally but not paternally derived proximal 15q duplicationNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsInfant siblings and the investigation of autism risk factorsParent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.Autism spectrum disorder and epileptic encephalopathy: common causes, many questions.Transmission disequilibrium testing of the chromosome 15q11-q13 region in autismAssessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.A genomewide screen for autism susceptibility loci.Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autismA quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disordersRecurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium studyGenetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder.Autism risk assessment in siblings of affected children using sex-specific genetic scores.Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.Maternal transmission of a rare GABRB3 signal peptide variant is associated with autismRYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autism.Early social, imitation, play, and language abilities of young non-autistic siblings of children with autism.Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersThe power and promise of identifying autism early: insights from the search for clinical and biological markers.SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowthPathogenesis of autism: a patchwork of genetic causes.A nationwide study of the association between celiac disease and the risk of autistic spectrum disorders.Dynamic Akt/mTOR Signaling in Children with Autism Spectrum DisorderCandidate Genes for Inherited Autism Susceptibility in the Lebanese Population.Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder.The pathophysiology of restricted repetitive behavior.Detecting, studying, and treating autism early: the one-year well-baby check-up approach.
P2860
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P2860
description
1991 nî lūn-bûn
@nan
1991 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Complex segregation analysis of autism.
@ast
Complex segregation analysis of autism.
@en
type
label
Complex segregation analysis of autism.
@ast
Complex segregation analysis of autism.
@en
prefLabel
Complex segregation analysis of autism.
@ast
Complex segregation analysis of autism.
@en
P2093
P2860
P1476
Complex segregation analysis of autism.
@en
P2093
A Mason-Brothers
B J Freeman
B Petersen
S J Hasstedt
W M McMahon
W R Jenson
P2860
P304
P407
P577
1991-11-01T00:00:00Z