Copy number variation in Han Chinese individuals with autism spectrum disorder. - Wikidata - awgldk - TriplyDB

Copy number variation in Han Chinese individuals with autism spectrum disorder.

Copy number variation in Han Chinese individuals with autism spectrum disorder.

http://www.wikidata.org/entity/Q34101228

about

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Clinically relevant copy number variations detected in cerebral palsy Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.De novo genic mutations among a Chinese autism spectrum disorder cohort.Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.The Physiological, Biochemical, and Molecular Roles of Zinc Transporters in Zinc Homeostasis and Metabolism.A GluD Coming-Of-Age Story.Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3.Long non-coding RNA NAP1L6 promotes tumor progression and predicts poor prognosis in prostate cancer by targeting Inhibin-β A

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P2860

Copy number variation in Han Chinese individuals with autism spectrum disorder.

http://www.wikidata.org/entity/Q34101228

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին 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

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@ast

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@en

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@nl

type

label

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@ast

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@en

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@nl

prefLabel

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@ast

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@en

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@nl

P1433

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P1433

Journal of Neurodevelopmental Disorders

P1476

Copy number variation in Han Chinese individuals with autism spectrum disorder.

@en

P2093

Anath C Lionel

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

Caihong Sun

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

Jia Wang

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

John Wei

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

Lijie Wu

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

Matthew J Gazzellone

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

Mingyang Zou

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

Mohammed Uddin

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

Shuang Liang

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

Susan Walker

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

P2860

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

Large, rare chromosomal deletions associated with severe early-onset obesity

Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease

Structural variation of chromosomes in autism spectrum disorder

Tandem SAM Domain Structure of Human Caskin1: A Presynaptic, Self-Assembling Scaffold for CASK

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome

Global prevalence of autism and other pervasive developmental disorders

Neurulation and neurite extension require the zinc transporter ZIP12 (slc39a12)

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

P2888

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34

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scholarly article

P356

10.1186/1866-1955-6-34

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1

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6

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Bhooma Thiruvahindrapuram

Kristiina Tammimies

Stephen W. Scherer

P577

2014-08-23T00:00:00Z

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265174908

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1035214646

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25170348

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P921

Autism spectrum

P932

4147384

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