Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome

Author(s):
Kuiper, R.P.; Vissers, L.E.L.M.; Venkatachalam, R.; Bodmer, D.; Hoenselaar, E.; Goossens, M.; Haufe, A.; Kamping, E.; Niessen, R.C.; Hogervorst, F.B.L.; Gille, J.J.P.; Redeker, B.; Tops, C.M.J.; Gijn, M.E. van; Ouweland, A.M.W. van den; Rahner, N.; Steinke, V.; Kahl, P.; Holinski-Feder, E.; Morak, M.; Kloor, M.; Stemmler, S.; Betz, B.; Hutter, P.; Bunyan, D.J.; Syngal, S.; Culver, J.O.; Graham, T.; Chan, T.L.; Nagtegaal, I.D.; Krieken, J.H.J.M. van; Schackert, H.K.; Hoogerbrugge, N.; Kessel, A.G. van; Ligtenberg, M.J.L.
Published
2011
Publication type
Article / Letter to editor
Lynch syndromeEPCAMTACSTD1NAHRAlu-mediated recombination
Date issued
2011-04-30
Language
English
Is part of
Human Mutation (2011), Vol. 32, no. 4, p. 407-414
hdl
1887/118290
doi
10.1002/humu.21446