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- 2022
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Mark
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield : Results from a nationwide prospective cohort
(
- Contribution to journal › Article
- 2017
-
Mark
Genetic anticipation in Swedish Lynch syndrome families
(
- Contribution to journal › Article
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Mark
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
(
- Contribution to journal › Article
- 2014
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Mark
Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein.
(
- Contribution to journal › Article
- 2009
-
Mark
Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels
(
- Contribution to journal › Article
- 2008
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Mark
Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72
(
- Contribution to journal › Article
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Mark
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
(
- Contribution to journal › Article
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Mark
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
(
- Contribution to journal › Article
- 2007
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Mark
Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer
(
- Contribution to journal › Article
- 2006
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Mark
Long-range PCR facilitates the identification of PMS2-specific mutations
(
- Contribution to journal › Article