Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

HM Van Der Klift; AR Mensenkamp; M Drost; E C Bik; YJ Vos; HJJP Gille; Bejw Redeker; Y Tiersma; JBM Zonneveld; EG Garcia; TGW Letteboer; M J W Olderode-Berends; LP van Hest; TA van Os; S Verhoef; Anja Wagner; CJ van Asperen; SW ten Broeke; FJ Hes; N de Wind; M Nielsen; P Devilee; MJL Ligtenberg; JT Wijnen; CMJ Tops

doi:10.1002/humu.23052

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

HM Van Der Klift
, AR Mensenkamp
, M Drost
, E C Bik
, YJ Vos
, HJJP Gille
, Bejw Redeker
, Y Tiersma
, JBM Zonneveld
, EG Garcia
, TGW Letteboer
, M J W Olderode-Berends
, LP van Hest
, TA van Os
, S Verhoef
, Anja Wagner
, CJ van Asperen
, SW ten Broeke
, FJ Hes
, N de Wind

M Nielsen, P Devilee, MJL Ligtenberg, JT Wijnen, CMJ Tops

Clinical Genetics

Research output: Contribution to journal › Article › Academic › peer-review

57 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1162-1179
Number of pages	18
Journal	Human Mutation
Volume	37
Issue number	11
DOIs	https://doi.org/10.1002/humu.23052
Publication status	Published - 2016

Research programs

EMC MGC-02-96-01

Access to Document

10.1002/humu.23052

Cite this

Van Der Klift, HM., Mensenkamp, AR., Drost, M., Bik, E. C., Vos, YJ., Gille, HJJP., Redeker, B., Tiersma, Y., Zonneveld, JBM., Garcia, EG., Letteboer, TGW., Olderode-Berends, M. J. W., van Hest, LP., van Os, TA., Verhoef, S., Wagner, A., van Asperen, CJ., ten Broeke, SW., Hes, FJ., ... Tops, CMJ. (2016). Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome. Human Mutation, 37(11), 1162-1179. https://doi.org/10.1002/humu.23052

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year = "2016",

doi = "10.1002/humu.23052",

language = "Undefined/Unknown",

volume = "37",

pages = "1162--1179",

journal = "Human Mutation",

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Van Der Klift, HM, Mensenkamp, AR, Drost, M, Bik, EC, Vos, YJ, Gille, HJJP, Redeker, B, Tiersma, Y, Zonneveld, JBM, Garcia, EG, Letteboer, TGW, Olderode-Berends, MJW, van Hest, LP, van Os, TA, Verhoef, S, Wagner, A, van Asperen, CJ, ten Broeke, SW, Hes, FJ, de Wind, N, Nielsen, M, Devilee, P, Ligtenberg, MJL, Wijnen, JT & Tops, CMJ 2016, 'Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome', Human Mutation, vol. 37, no. 11, pp. 1162-1179. https://doi.org/10.1002/humu.23052

TY - JOUR

T1 - Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

AU - Van Der Klift, HM

AU - Mensenkamp, AR

AU - Drost, M

AU - Bik, E C

AU - Vos, YJ

AU - Gille, HJJP

AU - Redeker, Bejw

AU - Tiersma, Y

AU - Zonneveld, JBM

AU - Garcia, EG

AU - Letteboer, TGW

AU - Olderode-Berends, M J W

AU - van Hest, LP

AU - van Os, TA

AU - Verhoef, S

AU - Wagner, Anja

AU - van Asperen, CJ

AU - ten Broeke, SW

AU - Hes, FJ

AU - de Wind, N

AU - Nielsen, M

AU - Devilee, P

AU - Ligtenberg, MJL

AU - Wijnen, JT

AU - Tops, CMJ

PY - 2016

Y1 - 2016

U2 - 10.1002/humu.23052

DO - 10.1002/humu.23052

M3 - Article

SN - 1059-7794

VL - 37

SP - 1162

EP - 1179

JO - Human Mutation

JF - Human Mutation

IS - 11

ER -