Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression

M. Clendenning, Fa Macrae, Md Walsh, R. J. Walters, Stephen N Thibodeau, S. R. Gunawardena, J. D. Potter, R. W. Haile, S. Gallinger, J. L. Hopper, M. A. Jenkins, C. Rosty, J. P. Young, D. D. Buchanan

Research output: Contribution to journalArticle

7 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)591-593
Number of pages3
JournalClinical Genetics
Volume83
Issue number6
DOIs
StatePublished - Jun 2013

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Signal Transducing Adaptor Proteins
DNA Mutational Analysis
DNA Repair Enzymes
DNA-Binding Proteins
Nuclear Proteins
Adenosine Triphosphatases
Registries
Colorectal Neoplasms
Colon
Cohort Studies
Immunohistochemistry
High Pressure Liquid Chromatography
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression. / Clendenning, M.; Macrae, Fa; Walsh, Md; Walters, R. J.; Thibodeau, Stephen N; Gunawardena, S. R.; Potter, J. D.; Haile, R. W.; Gallinger, S.; Hopper, J. L.; Jenkins, M. A.; Rosty, C.; Young, J. P.; Buchanan, D. D.

In: Clinical Genetics, Vol. 83, No. 6, 06.2013, p. 591-593.

Research output: Contribution to journalArticle

Clendenning, M, Macrae, F, Walsh, M, Walters, RJ, Thibodeau, SN, Gunawardena, SR, Potter, JD, Haile, RW, Gallinger, S, Hopper, JL, Jenkins, MA, Rosty, C, Young, JP & Buchanan, DD 2013, 'Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression', Clinical Genetics, vol. 83, no. 6, pp. 591-593. https://doi.org/10.1111/cge.12011
Clendenning, M. ; Macrae, Fa ; Walsh, Md ; Walters, R. J. ; Thibodeau, Stephen N ; Gunawardena, S. R. ; Potter, J. D. ; Haile, R. W. ; Gallinger, S. ; Hopper, J. L. ; Jenkins, M. A. ; Rosty, C. ; Young, J. P. ; Buchanan, D. D. / Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression. In: Clinical Genetics. 2013 ; Vol. 83, No. 6. pp. 591-593.
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