Leiden University Scholarly Publications

Your Search

Enabled Filters

  • (-) = Lynch syndrome
  • (-) ≠ Ligtenberg, M.J.L.
  • (-) = Hes, F.J.

Refine Results

Resource Type

Availability

Creation Date

Faculty

Collection

Topic

Author

Language

Search results

  • RSS Feed
(1 - 4 of 4)
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Suerink, M.; Klift, H.M. van der; Broeke, S.W. ten; Dekkers, O.M.; Bernstein, I.; Munar, G.C.; ... ; Nielsen, M. 2016
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Article / Letter to editor
open access
Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer
Bosse, T.; Haar, N.T. ter; Seeber, L.M.; Diest, P.J. van; Hes, F.J.; Vasen, H.F.A.; ... ; Smit, V.T.H.B.M. 2013
Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer
Article / Letter to editor
metadata only
Value-based healthcare in Lynch syndrome
Hennink, S.D.; Hofland, N.; Gopie, J.P.; Kaa, C. van der; Koning, K. de; Nielsen, M.; ... ; Vasen, H.F.A. 2013
Value-based healthcare in Lynch syndrome
Article / Letter to editor
metadata only
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome
Klift, H.M.D. van der; Tops, C.M.; Hes, F.J.; Devilee, P.; Wijnen, J.T. 2012
Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of lynch syndrome
Article / Letter to editor
metadata only