about
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genesThe genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderGenetics of austim: complex aetiology for a heterogeneous disorderLinkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneAllelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsExcess 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 impairmentA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Genome-wide linkage analyses of quantitative and categorical autism subphenotypesAbsence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaGenome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlatesMutation screening and imprinting analysis of four candidate genes for autism in the 7q32 regionGenome-wide scan for loci of Asperger syndromeParent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.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.Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.Evaluation of FOXP2 as an autism susceptibility gene.Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.A genomewide screen for autism susceptibility loci.A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Imprinted genes and mental dysfunction.Investigation of two variants in the DOPA decarboxylase gene in patients with autism.The genetics of autism.Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairmentDefining the contribution of CNTNAP2 to autism susceptibility.Accuracy of phenotyping of autistic children based on Internet implemented parent report.Disease susceptibility genes for autism.Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibilityMolecular genetics of autism spectrum disorder.Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autismLinks between genetics and pathophysiology in the autism spectrum disorders.Mutations in the TSGA14 gene in families with autism spectrum disorders.William's syndrome: gene expression is related to parental origin and regional coordinate control.Early pharmacological treatment of autism: a rationale for developmental treatment.Linkage and association of the glutamate receptor 6 gene with autism.
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին 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
Genetic studies of autistic disorder and chromosome 7
@ast
Genetic studies of autistic disorder and chromosome 7
@en
Genetic studies of autistic disorder and chromosome 7
@nl
type
label
Genetic studies of autistic disorder and chromosome 7
@ast
Genetic studies of autistic disorder and chromosome 7
@en
Genetic studies of autistic disorder and chromosome 7
@nl
prefLabel
Genetic studies of autistic disorder and chromosome 7
@ast
Genetic studies of autistic disorder and chromosome 7
@en
Genetic studies of autistic disorder and chromosome 7
@nl
P2093
P356
P1433
P1476
Genetic studies of autistic disorder and chromosome 7
@en
P2093
A Ashley-Koch
A S Aylsworth
C M Powell
C M Wolpert
G R DeLong
H H Wright
J R Gilbert
M A Pericak-Vance
P304
P356
10.1006/GENO.1999.5968
P407
P577
1999-11-01T00:00:00Z