Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations

Author(s):
Leenen, C.H.M.; Geurts-Giele, W.R.R.; Dubbink, H.J.; Reddingius, R.; Ouweland, A.M. van den; Tops, C.M.J.; Klift, H.M. van de; Kuipers, E.J.; Leerdam, M.E. van (0000-0002-5719-3208); Dinjens, W.N.M.; Wagner, A.
Published
2011
Publication type
Article / Letter to editor
compound heterozygosityconstitutional mismatch repair deficiencyimmunohistochemistryLynch syndromemicrosatellite instabilityPMS2
Date issued
2011-12-31
Language
English
Is part of
Clinical Genetics (2011), Vol. 80, no. 6, p. 558-565
hdl
1887/109870
doi
10.1111/j.1399-0004.2010.01608.x