Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes Meeting Abstract (Web of Science)

cited authors

  • Waldron, John; Termine, Kirsten W.; Musolf, Anthony M.; de Andrade, Mariza; Gaba, Colette; Govindan, Ramaswamy; Yang, Ping; You, Ming; Jaeger, Ellen; Bencaz, Angelle F.; Anderson, Marshall W.; Schwartz, Ann G.; Pinney, Susan M.; Amos, Christopher I.; Bailey-Wilson, Joan E.; Mandal, Diptasri M.

publication date

  • June 15, 2022


published in



  • 82


  • 12