Genomic copy-number variations (CNVs) involving large DNA segments are known to cause many genetic disorders. Depending on the changes, they are predicted to lead either to decreased or an increased gene expression. However, the ability to detect smaller exonic copy-number changes has not been explo
Oligonucleotide-array–based comparative genomic hybridization
✍ Scribed by Baldocchi, R.A.; Glynne, R.J.; Kowbel, D.; Tom, E.; Collins, C.; Mack, D.H.; Gray, J.W.
- Book ID
- 109525830
- Publisher
- Nature Publishing Group
- Year
- 1999
- Tongue
- English
- Weight
- 114 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1061-4036
- DOI
- 10.1038/14265
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