Rare germline copy number variants in colorectal cancer predisposition characterized by exome sequencing analysis

J Genet Genomics. 2018 Jan 20;45(1):41-45. doi: 10.1016/j.jgg.2017.12.001. Epub 2017 Dec 20.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • DNA Copy Number Variations / genetics*
  • Exome / genetics
  • Exome Sequencing
  • Genetic Predisposition to Disease*
  • Germ Cells
  • High-Throughput Nucleotide Sequencing
  • Humans