(Q36737126)

English

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

scientific article published on February 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

0 references

1 reference

Europe PubMed Central

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

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

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systematic review

1 reference

based on heuristic

inferred from title

learning disability

1 reference

based on heuristic

inferred from title

Gurdeep S Sagoo

object named as

Gurdeep Sagoo

3

0 references

object named as

Julian Higgins

4

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5

object named as

Hilary Burton

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

7

object named as

Mark Kroese

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

author name string

Subu Subramonia-Iyer

1

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Simon Sanderson

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Ron Zimmern

6

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Pippa Brice

8

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Charles Shaw-Smith

9

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

language of work or name

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publication date

1 February 2007

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Europe PubMed Central

PubMed publication ID

16 August 2017

Genetics in Medicine

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Europe PubMed Central

PubMed publication ID

16 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

74-79

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

https://scigraph.springernature.com/pub.10.1097/gim.0b013e31803141f2

0 references

Advances in molecular cytogenetics for the evaluation of mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

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.0B013E31803141F2

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.0B013E31803141F2

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Genetic tests and their evaluation: can we answer the key questions?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Quantifying heterogeneity in a meta-analysis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Measuring inconsistency in meta-analyses

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

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.0B013E31803141F2

21 January 2018

Diagnostic genome profiling in mental retardation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

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.0B013E31803141F2

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.0B013E31803141F2

21 January 2018

Being sceptical about meta-analyses: a Bayesian perspective on magnesium trials in myocardial infarction.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Comparative accuracy: assessing new tests against existing diagnostic pathways

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

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.0B013E31803141F2

21 January 2018

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31803141F2

21 January 2018

Identifiers

10.1097/GIM.0B013E31803141F2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

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