Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

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Wolf-Hirschhorn Syndrome Candidate 1 Is Necessary for Correct Hematopoietic and B Cell Development.

P2860

Q45868105-8C4D577C-22B6-4911-B80D-797ADBA83889

P2860

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

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http://www.wikidata.org/entity/Q34694684

description

2010 nî lūn-bûn

@nan

2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

@ast

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

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Clinical utility gene card for: Wolf-Hirschhorn

@nl

type

Item

label

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

@ast

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

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Clinical utility gene card for: Wolf-Hirschhorn

@nl

prefLabel

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

@ast

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

@en

Clinical utility gene card for: Wolf-Hirschhorn

@nl

P1476

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

@en

P2093

Agatino Battaglia

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

John C Carey

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

Sarah South

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

P2860

Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

Wolf-Hirschhorn (4p-) syndrome.

Seizure and EEG patterns in Wolf-Hirschhorn (4p-) syndrome.

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation.

On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.

A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome.

Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.

Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH).

Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.

P2888

ejhg.2010.186

P304

458-464

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P31

scholarly article

P356

10.1038/EJHG.2010.186

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P478

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

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2010-12-08T00:00:00Z

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49676659

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P698

21150881

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P932

3060313

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Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

about

P2860

P2860

Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P698

P932