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(1 - 3 of 3)
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers
Goverde, A.; Spaander, M.C.W.; Nieboer, D.; Ouweland, A.M.W. van den; Dinjens, W.N.M.; Dubbink, H.J.; ... ; Wagner, A. 2018
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers
Article / Letter to editor
open access
Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future
Rasmussen, L.J.; Heinen, C.D.; Royer-Pokora, B.; Drost, M.; Tavtigian, S.; Hofstra, R.M.W.; Wind, N. de 2012
Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future
Article / Letter to editor
metadata only
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants
Drost, M.; Zonneveld, J.B.; Hees, S. van; Rasmussen, L.J.; Hofstra, R.M.W.; Wind, N. de 2012
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants
Article / Letter to editor
metadata only