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Relative burden of large CNVs on a range of neurodevelopmental phenotypes

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313522950

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

About this item

Full title

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

Publisher

United States: Public Library of Science

Journal title

PLoS genetics, 2011-11, Vol.7 (11), p.e1002334

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

While numerous studies have implicated copy number variants (CNVs) in a range of neurological phenotypes, the impact relative to disease severity has been difficult to ascertain due to small sample sizes, lack of phenotypic details, and heterogeneity in platforms used for discovery. Using a customized microarray enriched for genomic hotspots, we as...

Alternative Titles

Full title

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1313522950

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313522950

Other Identifiers

ISSN

1553-7404,1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1002334

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