HKU Scholars Hub: Browsing DSpace

Browsing by Author Bodmer, D

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 1 to 3 of 3

	Title	Author(s)	Issue Date
	A novel cause of Lynch syndrome: heritable somatic methylation of MSH2 due to deletion of the 30 exons of the upstream gene Proceeding/Conference:Familial Cancer	Ligtenberg, MJL Kuiper, RP Chan, TL Goossens, M Hebeda, KM Voorendt, M Bodmer, D Hoenselaar, E Hendriks-Cornelissen, SJB Brunner, HG Geurts van Kessel, A van Krieken, JHJM Leung, SY Hoogerbrugge, N	2010
	Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 Journal:Nature Genetics	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
	Recurrence and variability of germline EPCAM deletions in Lynch syndrome Journal:Human Mutation	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

Showing results 1 to 3 of 3