about
A clinical and neurobehavioural review of high-functioning autism and Asperger's disorderA genomewide screen of 345 families for autism-susceptibility loci.A genomic screen of autism: evidence for a multilocus etiology.On the twin risk in autismCurrent developments in the genetics of autism: from phenome to genomeA genetic study of autism in Costa Rica: multiple variables affecting IQ scores observed in a preliminary sample of autistic casesValidation of the diagnosis of autism in general practitioner recordsA Short Review on the Current Understanding of Autism Spectrum DisordersImprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autismLack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex familiesAssociation studies of the HOPA dodecamer duplication variant in different subtypes of autismAutism and serotonin transporter gene polymorphisms: a systematic review and meta-analysisAssociation of the neuronal cell adhesion molecule (NRCAM) gene variants with autismAnalysis of the RELN gene as a genetic risk factor for autismInfant siblings and the investigation of autism risk factorsSociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in miceAutism.Current topic: Screening and surveillance for autism and pervasive developmental disorders.Genetic and neurodevelopmental influences in autistic disorder.An investigation of ribosomal protein L10 gene in autism spectrum disorders.Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.A pilot study of maternal sensitivity in the context of emergent autism.The use of genetic epidemiology to guide classification in child and adult psychopathology.Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.The familial risk of autism.A genomewide screen for autism susceptibility loci.A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Predicting social impairment and ASD diagnosis in younger siblings of children with autism spectrum disorder.The timing and specificity of prenatal immune risk factors for autism modeled in the mouse and relevance to schizophrenia.The effects of birth order and birth interval on the phenotypic expression of autism spectrum disorder.Change in maternal criticism and behavior problems in adolescents and adults with autism across a 7-year period.Sex-specific rates of transmission of psychosis in the New England high-risk family study.Pragmatic language and school related linguistic abilities in siblings of children with autism.Disease susceptibility genes for autism.Prenatal and neonatal thyroid stimulating hormone levels and autism spectrum disorders.Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.Variation in vocal-motor development in infant siblings of children with autism
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
Genetics of autism: overview and new directions.
@en
Genetics of autism: overview and new directions.
@nl
type
label
Genetics of autism: overview and new directions.
@en
Genetics of autism: overview and new directions.
@nl
prefLabel
Genetics of autism: overview and new directions.
@en
Genetics of autism: overview and new directions.
@nl
P2093
P356
P1476
Genetics of autism: overview and new directions.
@en
P2093
L Zwaigenbaum
P Szatmari
P2888
P304
P356
10.1023/A:1026096203946
P407
P577
1998-10-01T00:00:00Z
P6179
1043368433