Molecular-neurobehavioral associations in females with the fragile X full mutation.
about
Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1Molecular and cellular genetics of fragile X syndrome.Prevalence, nature, and correlates of sleep problems among children with fragile X syndrome based on a large scale parent survey.Advances in research on the fragile X syndrome.Fragile X syndrome. Molecular and clinical insights and treatment issuesA developmental approach to understanding Fragile X syndrome in females.Resolution of spatial and temporal visual attention in infants with fragile X syndrome.Mental status of females with an FMR1 gene full mutationFear-specific amygdala function in children and adolescents on the fragile x spectrum: a dosage response of the FMR1 gene.Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome.A controlled study of longitudinal IQ changes in females and males with fragile X syndrome.Screening for fragile X syndrome: information needs for health planners.Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.Preliminary evidence for a cognitive phenotype in Barth syndrome.Prevalence of the fragile X syndrome in African-Americans.Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief report.FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome.Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling.Do anomalies of handedness exist in children with Fragile-X syndrome?Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators.Contribution of the FMR1 gene mutation to human intellectual dysfunction.Seventh International Workshop on the Fragile X and X-linked Mental Retardation.Genetic and maternal predictors of cognitive and behavioral trajectories in females with fragile X syndrome.
P2860
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P2860
Molecular-neurobehavioral associations in females with the fragile X full mutation.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh-hant
name
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@en
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@nl
type
label
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@en
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@nl
prefLabel
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@en
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@nl
P2093
P356
P1476
Molecular-neurobehavioral associations in females with the fragile X full mutation.
@en
P2093
P2860
P304
P356
10.1002/AJMG.1320510407
P577
1994-07-01T00:00:00Z