Genetics in Medicine Open (Jan 2023)

P582: Exon-level copy number variations identified by whole genome sequencing in previously undiagnosed patients with rare hereditary diseases

  • Jiyong Wang,
  • Raymond Caylor,
  • Julie Jones,
  • Jennifer Lee,
  • Raymond Louie,
  • Benjamin Hilton,
  • Barbara DuPont,
  • Kameryn Butler

Journal volume & issue
Vol. 1, no. 1
p. 100629

Abstract

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No abstracts available.