An autosomal genomic screen for autism. Collaborative linkage study of autism
about
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryAssociation of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisLinkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneReplication of autism linkage: fine-mapping peak at 17q21.Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsA genomewide screen of 345 families for autism-susceptibility loci.The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditionsExcess of twins among affected sibling pairs with autism: implications for the etiology of autism.Chromosome 7q: where autism meets language disorder?Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderFOXP2 is not a major susceptibility gene for autism or specific language impairmentOn the twin risk in autismA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Rapid automatized naming as an index of genetic liability to autismExamination of association of genes in the serotonin system to autismCurrent developments in the genetics of autism: from phenome to genomeGenome-wide linkage analyses of quantitative and categorical autism subphenotypesA genetic variant that disrupts MET transcription is associated with autismGenome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlatesCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderObservation of Spontaneous Expressive Language (OSEL): a new measure for spontaneous and expressive language of children with autism spectrum disorders and other communication disordersMicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.Decreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal DiseaseMouse behavioral tasks relevant to autism: phenotypes of 10 inbred strainsThe autism diagnosis in translation: shared affect in children and mouse models of ASD.A Genetic Multimutation Model of Autism Spectrum Disorder Fits Disparate Twin Concordance Data from the USA and CanadaConsanguinity mapping of congenital heart disease in a South Indian population.Genome-wide linkage in Utah autism pedigreesCommunication, interventions, and scientific advances in autism: a commentary.Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.Association of specific language impairment (SLI) to the region of 7q31.All LODs are not created equal.Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment.Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.A genomewide screen for autism susceptibility loci.Investigation of two variants in the DOPA decarboxylase gene in patients with autism.Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.Examination of association to autism of common genetic variationin genes related to dopamine.
P2860
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P2860
An autosomal genomic screen for autism. Collaborative linkage study of autism
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
An autosomal genomic screen for autism. Collaborative linkage study of autism
@ast
An autosomal genomic screen for autism. Collaborative linkage study of autism
@en
An autosomal genomic screen for autism. Collaborative linkage study of autism
@nl
type
label
An autosomal genomic screen for autism. Collaborative linkage study of autism
@ast
An autosomal genomic screen for autism. Collaborative linkage study of autism
@en
An autosomal genomic screen for autism. Collaborative linkage study of autism
@nl
prefLabel
An autosomal genomic screen for autism. Collaborative linkage study of autism
@ast
An autosomal genomic screen for autism. Collaborative linkage study of autism
@en
An autosomal genomic screen for autism. Collaborative linkage study of autism
@nl
P2093
P1476
An autosomal genomic screen for autism. Collaborative linkage study of autism
@en
P2093
D Childress
D Y Nishimura
J A Mullane
J Singleton
P304
P407
P577
1999-12-15T00:00:00Z