Copy Number Variants in the Kallikrein Gene Cluster
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference25 articles.
1. Genome structural variation discovery and genotyping;C Alkan;Nat Rev Genet,2011
2. Origins and functional impact of copy number variation in the human genome;DF Conrad;Nature,2010
3. Mutation spectrum revealed by breakpoint sequencing of human germline CNVs;DF Conrad;Nat Genet,2010
4. Phenotypic impact of genomic structural variation: insights from and for human disease;J Weischenfeldt;Nat Rev Genet,2013
5. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls;N Craddock;Nature,2010
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A computational analysis of the genetic and transcript diversity at the kallikrein locus;Biological Chemistry;2016-12-01
2. Genotyping of common SIRPB1 copy number variant using Paralogue Ratio Test coupled to MALDI-MS quantification;Molecular and Cellular Probes;2015-12
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