| Title | Author(s) | Year | View Count |
 | Recurrence and variability of germline EPCAM deletions in Lynch syndrome | Kuiper, RP; Vissers, LELM; Venkatachalam, R; Bodmer, D; Hoenselaar, E; Goossens, M; Haufe, A; Kamping, E; Niessen, RC; Hogervorst, FBL; Gille, JJP; Redeker, B; Tops, CMJ; van Gijn, ME; van den Ouweland, AMW; Rahner, N; Steinke, V; Kahl, P; HolinskiFeder, E; Morak, M; Kloor, M; Stemmler, S; Betz, B; Hutter, P; Bunyan, DJ; Syngal, S; Culver, JO; Graham, T; Chan, TL; Nagtegaal, ID; van Krieken, JHJM; Schackert, HK; Hoogerbrugge, N; van Kessel, AG; Ligtenberg, MJL | 2011 | 101 |
| Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 | Ligtenberg, MJL; Kuiper, RP; Chan, TL; Goossens, M; Hebeda, KM; Voorendt, M; Lee, TYH; Bodmer, D; Hoenselaar, E; HendriksCornelissen, SJB; Tsui, WY; Kong, CK; Brunner, HG; Van Kessel, AG; Yuen, ST; Van Krieken, JHJM; Leung, SY; Hoogerbrugge, N | 2009 | 66 |
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