Skip to main content
Leiden University
Scholarly Publications
Home
Submit
About
Select Collection
All collections
Academic speeches
Dissertations
Faculty of Archaeology
Faculty of Governance and Global Affairs
Faculty of Humanities
Faculty of Science
Faculty of Social and Behavioural Sciences
Leiden Journals, Conference Proceedings and Books
Leiden Law School
Leiden University Press
Medicine / Leiden University Medical Centre (LUMC)
Research output UL
Search box
Your Search
Enabled Filters
(-)
= Thompson, B.A.
Sort Options
Date (year)
Author / Creator
Title
Refine Results
Resource Type
Article / Letter to editor
(6)
+
-
Availability
Open access
(2)
+
-
Metadata Only
(4)
+
-
Creation Date
2020
(2)
+
-
Faculty
Leiden University Medical Center (LUMC)
(6)
+
-
Collection
Medicine / Leiden University Medical Centre (LUMC)
(6)
+
-
Topic
Lynch syndrome
(3)
+
-
variants of uncertain significance
(2)
+
-
Author
Spurdle, A.B.
(6)
+
-
Thompson, B.A.
(6)
+
-
Drost, M.
(5)
+
-
Tavtigian, S.V.
(5)
+
-
Wind, N. de
(5)
+
-
Greenblatt, M.S.
(4)
+
-
Rasmussen, L.J.
(4)
+
-
Tiersma, Y.
(4)
+
-
Boucher, K.M.
(3)
+
-
Glubb, D.
(3)
+
-
Goldgar, D.E.
(3)
+
-
Kathe, S.
(3)
+
-
Asperen, C.J. van
(2)
+
-
Frederiksen, J.H.
(2)
+
-
Keijzers, G.
(2)
+
-
Molenkamp, S.
(2)
+
-
Osinga, J.
(2)
+
-
Pappas, L.
(2)
+
-
Parsons, M.T.
(2)
+
-
Sijmons, R.H.
(2)
+
-
Wallace, S.S.
(2)
+
-
Westers, H.
(2)
+
-
Zonneveld, J.B.
(2)
+
-
Show more
Language
en
(6)
+
-
Search results
(1 - 6 of 6)
show grid
show list
save search
Contribution of mRNA splicing to mismatch repair gene sequence variant interpretation
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database