Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication. - Wikidata - awgldk - TriplyDB

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

http://www.wikidata.org/entity/Q33554172

about

From Genetics to Epigenetics: New Perspectives in Tourette Syndrome Research Genetics of obsessive-compulsive disorder and related disorders.Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study Tics and shorter stature: should we be looking for an association?CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.The genetics of Tourette disorder MicroRNA Profiling of Neurons Generated Using Induced Pluripotent Stem Cells Derived from Patients with Schizophrenia and Schizoaffective Disorder, and 22q11.2 Del.Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.Episodic Behavioural Regression in an 8-Year-Old Female: Sequelae of 22q11.2 Duplication Syndrome

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Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

http://www.wikidata.org/entity/Q33554172

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@ast

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@en

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@nl

type

label

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@ast

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@en

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@nl

prefLabel

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@ast

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@en

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@nl

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P1433

Case Reports in Medicine

P1476

Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.

@en

P2093

Donald L Gilbert

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

Raymond A Clarke

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

Zhi Ming Fang

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

P2860

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

Abnormally increased CSF 3-Ortho-methyldopa (3-OMD) in untreated restless legs syndrome (RLS) patients indicates more severe disease and possibly abnormally increased dopamine synthesis

A common molecular basis for rearrangement disorders on chromosome 22q11

Tourette's syndrome: from behaviour to biology

Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

COMT polymorphisms and anxiety-related personality traits.

The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.

P304

361518

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scholarly article

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10.1155/2009/361518

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2009

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Ashish D. Diwan

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2009-12-22T00:00:00Z

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41001661

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20069037

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2797364

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