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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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Published in: | PloS one 2012-08, Vol.7 (8), p.e43466 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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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 ( |
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ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0043466 |