(Q50310312)

English

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

scientific article published on 26 September 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

medical genetics

0 references

author name string

Sarah T South

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Charles Lee

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Allen N Lamb

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Anne W Higgins

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Hutton M Kearney

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Working Group for the American College of Medical Genetics and Genomics Laboratory Quality Assurance Committee

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

language of work or name

0 references

publication date

26 September 2013

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

15

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

11

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

901-909

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

https://scigraph.springernature.com/pub.10.1038/gim.2013.129

0 references

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Towards an evidence-based process for the clinical interpretation of copy number variation

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Database resources of the National Center for Biotechnology Information

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Systematic biases in DNA copy number originate from isolation procedures

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

21 January 2018

Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2013.129

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/GIM.2013.129

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

release_otq35ytzqrff3g2n7z6phmphzq

1 reference

https://api.fatcat.wiki/v0/release/otq35ytzqrff3g2n7z6phmphzq

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24071793

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50310312&oldid=1838814057"