Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.
Welch JS; Westervelt P; Ding L; Larson DE; Klco JM; Kulkarni S; Wallis J; Chen K; Payton JE; Fulton RS; Veizer J; Schmidt H; Vickery TL; Heath S; Watson MA; Tomasson MH; Link DC; Graubert TA; DiPersio JF; Mardis ER; Ley TJ; Wilson RK; JAMA, 2011, vol. 305, issue 15, p 1577, ISSN 15383598. ISBN 15383598.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef