Genome-wide UPD screening in patients with intellectual disability - Wikidata - wikimedia - TriplyDB

Genome-wide UPD screening in patients with intellectual disability

Genome-wide UPD screening in patients with intellectual disability

http://www.wikidata.org/entity/Q34215703

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Genome-wide uniparental disomy screen in human discarded morphologically abnormal embryos.

P2860

Q35869302-56DFCCF6-E2AB-4F12-998E-FFA41264D05B

P2860

Genome-wide UPD screening in patients with intellectual disability

http://www.wikidata.org/entity/Q34215703

description

2014 nî lūn-bûn

@nan

2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի մայիսին 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

Genome-wide UPD screening in patients with intellectual disability

@ast

Genome-wide UPD screening in patients with intellectual disability

@en

Genome-wide UPD screening in patients with intellectual disability

@nl

type

label

Genome-wide UPD screening in patients with intellectual disability

@ast

Genome-wide UPD screening in patients with intellectual disability

@en

Genome-wide UPD screening in patients with intellectual disability

@nl

prefLabel

Genome-wide UPD screening in patients with intellectual disability

@ast

Genome-wide UPD screening in patients with intellectual disability

@en

Genome-wide UPD screening in patients with intellectual disability

@nl

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P1433

European Journal of Human Genetics

P1476

Genome-wide UPD screening in patients with intellectual disability

@en

P2093

Andreas Dufke

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

Angelika Riess

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

Arif Bülent Ekici

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

Christopher Schroeder

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

Gudrun Rappold

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

Marc Sturm

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

Michael Bonin

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

Sven Poths

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

Ulrike Mau-Holzmann

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

Ute Grasshoff

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

P2860

Mechanisms leading to uniparental disomy and their clinical consequences

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

Uniparental disomy analysis in trios using genome-wide SNP array and whole-genome sequencing data imply segmental uniparental isodisomy in general populations.

Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.

Clinical genetic evaluation of the child with mental retardation or developmental delays.

Cytogenetic contribution to uniparental disomy (UPD).

Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)

Global analysis of uniparental disomy using high density genotyping arrays.

Uniparental disomy and human disease: an overview.

Prevalence of intellectual disability: a meta-analysis of population-based studies.

P2888

P304

1233-1235

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scholarly article

P356

10.1038/EJHG.2014.63

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P433

10

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22

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P577

2014-05-07T00:00:00Z

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24801762

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P932

4169544

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