e-Article
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study
Document Type
Article
Author
Davidson, A.L.; Canson, D.M.; Glubb, D.M.; Fortuno, C.; Hollway, G.E.; Parsons, M.T.; Vidgen, M.E.; Holmes, O.; Koufariotis, L.T.; Lakis, V.; Leonard, C.; Wood, S.; Xu, Q.; Newell, F.; Tudini, E.; Pearson, J.V.; Spurdle, A.B.; Waddell, N.; Dressel, U.; Al-Shinnag, M.K.; Lau, C.; Mar Fan, H.G.; Ward, R.L.; Norris, S.; Austin, R.L.; McCart Reed, A.E.; Pickett, H.A.; Higgins, M.J.; Susman, R.D.; Troth, S.L.; Burke, J.; Mansour, J.L.; Millward, M.W.; Wallis, M.J.; Cops, E.J.; Trainer, A.H.; Walsh, M.; James, P.A.; Nichols, C.B.; Pachter, N.S.; Townshend, S.L.; Goodwin, A.; Harris, M.T.; Ip, E.L.; Kiraly-Borri, C.; Monnik, M.J.; Poplawski, N.K.; Ragunathan, A.; Winship, I.M.; Tucker, K.M.; Williams, R.A.
Source
In: Genome Medicine . (Genome Medicine, December 2023, 15(1))
Subject
Language
English
ISSN
1756994X