Digital Karyotyping with Whole Genomic Sequencing for Complex Congenital Disorder

J Genet Genomics. 2015 Nov 20;42(11):651-655. doi: 10.1016/j.jgg.2015.06.009. Epub 2015 Aug 6.
No abstract available

Publication types

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

MeSH terms

  • Congenital Abnormalities / genetics*
  • Female
  • Genome, Human*
  • Genomics
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Infant
  • Karyotyping
  • Proteins / genetics

Substances

  • Proteins