Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
- Published Article
Medycyna wieku rozwojowego
- Publication Date
Jan 01, 2012
Our study demonstrates that array comparative genomic hybridization enables detection of clinically significant chromosomal imbalances in patients with congenital heart defects.
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This record was last updated on 07/04/2016 and may not reflect the most current and accurate biomedical/scientific data available from NLM.
The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/23378395