Genomic studies in fragile X premutation carriers. - Wikidata - awgldk - TriplyDB

Genomic studies in fragile X premutation carriers.

Genomic studies in fragile X premutation carriers.

http://www.wikidata.org/entity/Q34101247

about

Fragile X spectrum disorders Fragile X-associated tremor/ataxia syndrome.Phenobarbital use and neurological problems in FMR1 premutation carriers Addictive substances may induce a rapid neurological deterioration in fragile X-associated tremor ataxia syndrome: A report of two cases Psychosis and catatonia in fragile X: Case report and literature review.Developmental profiles of infants with an FMR1 premutation.Aging in Fragile X Premutation Carriers.Fragile X syndrome: an overview and update of the FMR1 gene.Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families.FMR1 Premutation: Basic Mechanisms and Clinical Involvement.Fragile X-Associated Disorders in Serbia: Baseline Quantitative and Qualitative Survey of Knowledge, Attitudes and Practices Among Medical Professionals

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P2860

Genomic studies in fragile X premutation carriers.

http://www.wikidata.org/entity/Q34101247

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Genomic studies in fragile X premutation carriers.

@ast

Genomic studies in fragile X premutation carriers.

@en

Genomic studies in fragile X premutation carriers.

@nl

type

label

Genomic studies in fragile X premutation carriers.

@ast

Genomic studies in fragile X premutation carriers.

@en

Genomic studies in fragile X premutation carriers.

@nl

prefLabel

Genomic studies in fragile X premutation carriers.

@ast

Genomic studies in fragile X premutation carriers.

@en

Genomic studies in fragile X premutation carriers.

@nl

P1433

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P1433

Journal of Neurodevelopmental Disorders

P1476

Genomic studies in fragile X premutation carriers

@en

P2093

Evan E Eichler

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

Flora Tassone

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

Randi J Hagerman

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

Reymundo Lozano

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

P2860

Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population

De Novo Gene Disruptions in Children on the Autistic Spectrum

Missing heritability and strategies for finding the underlying causes of complex disease

Recent segmental duplications in the human genome

P2888

P304

27

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scholarly article

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10.1186/1866-1955-6-27

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1

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6

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Michael H Duyzend

Dejan B Budimirovic

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2014-07-30T00:00:00Z

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265213180

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4147387

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