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Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype

Whilst the majority of inherited diseases have been found to be caused by single base substitutions, small insertions or deletions (

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Bibliographic Details
Published in:PloS one 2012-08, Vol.7 (8), p.e43466
Main Authors: Carr, Ian M, Diggle, Christine P, Khan, Kamron, Inglehearn, Chris, McKibbin, Martin, Bonthron, David T, Markham, Alexander F, Anwar, Rashida, Dobbie, Angus, Pena, Sergio D J, Ali, Manir
Format: Article
Language:English
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Summary:Whilst the majority of inherited diseases have been found to be caused by single base substitutions, small insertions or deletions (
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0043466