about
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditionsCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderMatrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome.Infant siblings and the investigation of autism risk factorsEmotion potentiated startle in fragile X syndrome.Distinctive behavioral and cellular responses to fluoxetine in the mouse model for Fragile X syndrome.Genetic factors in child psychiatric disorders--II. Empirical findings.The psychiatric presentation of fragile x: evolution of the diagnosis and treatment of the psychiatric comorbidities of fragile X syndrome.The genetics of autism.Early development in males with Fragile X syndrome: a review of the literature.The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disordersFragile x syndrome and autism: from disease model to therapeutic targets.Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues.Complex segregation analysis of autism.Neuroanatomy in fragile X females: the posterior fossa.Parental inheritance and psychological disability in fragile X females.Annotation: fragile X syndrome: advances and controversy.Fragile X mental retardationPrevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum DisorderThe cyclic AMP phenotype of fragile X and autismThe genetics of child psychiatric disorders: focus on autism and Tourette syndrome.Development of mavoglurant and its potential for the treatment of fragile X syndrome.Autism: Oxytocin, serotonin, and social reward.The fragile X syndrome: implications of molecular genetics for the clinical syndrome.Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives.Inherited mental disorders.Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?Autism profiles of males with fragile X syndrome.Reduction of BDNF expression in Fmr1 knockout mice worsens cognitive deficits but improves hyperactivity and sensorimotor deficits.Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.Problems in the diagnosis of fragile X syndrome in young children are still present.Fragile X and autism.Physical characteristics of young boys with fragile X syndrome: reasons for difficulties in making a diagnosis in young males.[Characteristics of the communication in individuals with fragile X syndrome].Fragile X syndrome
P2860
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P2860
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Fragile X and autism: a multicenter survey.
@en
Fragile X and autism: a multicenter survey.
@nl
type
label
Fragile X and autism: a multicenter survey.
@en
Fragile X and autism: a multicenter survey.
@nl
prefLabel
Fragile X and autism: a multicenter survey.
@en
Fragile X and autism: a multicenter survey.
@nl
P2093
P2860
P356
P1476
Fragile X and autism: a multicenter survey
@en
P2093
A Mason-Brothers
E C Jenkins
E G Wolf-Schein
P2860
P304
P356
10.1002/AJMG.1320230126
P577
1986-01-01T00:00:00Z