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TypeTitleAuthor(s)YearViews
Recurrence and variability of germline EPCAM deletions in Lynch syndrome
Journal:
Human Mutation
Publisher:
John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/38515
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, MJL2011176
 
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
Journal:
Nature Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com
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, N2009172
 
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