Consistent count region–copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference33 articles.
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4. Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites;Brouwers;Mol Psychiatry,2012
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