Developmental profiles of infants with an FMR1 premutation.

about

Commentary: Depletion of the Fragile X Mental Retardation Protein in Embryonic Stem Cells Alters the Kinetics of Neurogenesis.Impact of Premutation on Neurobehavior and Bioenergetics in Young Monozygotic Twins Sensory Difficulties in Children With an FMR1 Premutation

P2860

Q37627065-0CC0CD66-F0AB-4062-BADB-B275287D3401 Q57167370-8422C485-F4A0-4261-A7D4-C6339736EB05 Q58697860-722DDB8B-56BB-4E73-B39E-FB13B2A33DBA

P2860

Developmental profiles of infants with an FMR1 premutation.

Item

http://www.wikidata.org/entity/Q37394408

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh

2016年學術文章

@zh-hant

name

Developmental profiles of infants with an FMR1 premutation.

@en

Developmental profiles of infants with an FMR1 premutation.

@nl

type

Item

label

Developmental profiles of infants with an FMR1 premutation.

@en

Developmental profiles of infants with an FMR1 premutation.

@nl

prefLabel

Developmental profiles of infants with an FMR1 premutation.

@en

Developmental profiles of infants with an FMR1 premutation.

@nl

P1476

Developmental profiles of infants with an FMR1 premutation.

@en

P2093

Anne C Wheeler

http://www.w3.org/2001/XMLSchema#string

Donald B Bailey

http://www.w3.org/2001/XMLSchema#string

Elizabeth Berry-Kravis

http://www.w3.org/2001/XMLSchema#string

Flora Tassone

http://www.w3.org/2001/XMLSchema#string

John Sideris

http://www.w3.org/2001/XMLSchema#string

Randi Hagerman

http://www.w3.org/2001/XMLSchema#string

P2860

A Meta-Analysis of Sensory Modulation Symptoms in Individuals with Autism Spectrum Disorders

Altered synaptic plasticity in a mouse model of fragile X mental retardation

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

Sensory Experiences Questionnaire: discriminating sensory features in young children with autism, developmental delays, and typical development

The mGluR theory of fragile X mental retardation

The neuroanatomy and neuroendocrinology of fragile X syndrome.

Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines.

CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.

CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

P2888

s11689-016-9171-8

P304

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1186/S11689-016-9171-8

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2016-11-03T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1008088778

http://www.w3.org/2001/XMLSchema#string

P698

27822316

http://www.w3.org/2001/XMLSchema#string

P932

5095966

http://www.w3.org/2001/XMLSchema#string

Developmental profiles of infants with an FMR1 premutation.

about

P2860

P2860

Developmental profiles of infants with an FMR1 premutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P577

P6179

P698

P932