(Q37444640)

English

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

scientific article published on March 2009

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 August 2017

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1 reference

Europe PubMed Central

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 August 2017

congenital disorder

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systematic review

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based on heuristic

inferred from title

learning disability

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based on heuristic

inferred from title

Gurdeep S Sagoo

object named as

Gurdeep S Sagoo

1

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Adam S. Butterworth

object named as

Adam S Butterworth

2

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5

object named as

Julian P T Higgins

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Europe PubMed Central

PubMed publication ID

20 August 2017

6

object named as

Hilary Burton

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Europe PubMed Central

PubMed publication ID

20 August 2017

author name string

Simon Sanderson

3

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Europe PubMed Central

PubMed publication ID

20 August 2017

Charles Shaw-Smith

4

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Europe PubMed Central

PubMed publication ID

20 August 2017

language of work or name

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publication date

1 March 2009

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Europe PubMed Central

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20 August 2017

Genetics in Medicine

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Europe PubMed Central

PubMed publication ID

20 August 2017

11

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Europe PubMed Central

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20 August 2017

3

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Europe PubMed Central

PubMed publication ID

20 August 2017

139-146

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Europe PubMed Central

PubMed publication ID

20 August 2017

https://scigraph.springernature.com/pub.10.1097/gim.0b013e318194ee8f

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Idiopathic learning disability and genome imbalance

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Array-based comparative genomic hybridization for investigating chromosomal abnormalities in patients with learning disability: systematic review meta-analysis of diagnostic and false-positive yields

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Measuring inconsistency in meta-analyses

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Operating characteristics of a rank correlation test for publication bias

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Bias in meta-analysis detected by a simple, graphical test

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318194EE8F

21 January 2018

Identifiers

10.1097/GIM.0B013E318194EE8F

1 reference

Europe PubMed Central

PubMed publication ID

20 August 2017

Dimensions Publication ID

0 references

release_dhtjcqxbfrd6lmlberwpdgfnxu

1 reference

https://api.fatcat.wiki/v0/release/dhtjcqxbfrd6lmlberwpdgfnxu

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 August 2017

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