Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort. - Wikidata - awgldk - TriplyDB

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

http://www.wikidata.org/entity/Q37692368

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LINE-1 Retrotransposons in Healthy and Diseased Human Brain.Genetic analysis of very obese children with autism spectrum disorder.A Review of Oxytocin and Arginine-Vasopressin Receptors and Their Modulation of Autism Spectrum Disorder.

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Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

http://www.wikidata.org/entity/Q37692368

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 10 March 2017

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@en

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

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type

label

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@en

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@nl

prefLabel

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@en

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@nl

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Scientific Reports

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Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

@en

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Fengyu Zhang

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

Guanglei Xun

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

Hui Guo

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

Jianjun Ou

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Jingjing Chen

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

Jingping Zhao

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Kun Xia

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Liangdan Sun

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Lu Shen

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

Lu Xia

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

P2860

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

NYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neurons

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

Functional impact of global rare copy number variation in autism spectrum disorders

Common genetic variants on 5p14.1 associate with autism spectrum disorders

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

Strong association of de novo copy number mutations with autism

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Structural variation of chromosomes in autism spectrum disorder

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44155

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scholarly article

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10.1038/SREP44155

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7

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2017-03-10T00:00:00Z

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28281572

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Autism spectrum

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5345089

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