|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
PMS2 monoallelic mutation carriers: the known unknown.
|
25856668 |
2016 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
|
26116798 |
2015 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
|
26318770 |
2015 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Structure of the MutLα C-terminal domain reveals how Mlh1 contributes to Pms1 endonuclease site.
|
23435383 |
2013 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
|
23709753 |
2013 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Four novel germline mutations in the MLH1 and PMS2 mismatch repair genes in patients with hereditary nonpolyposis colorectal cancer.
|
19479271 |
2009 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
|
18602922 |
2008 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
|
18602922 |
2008 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?
|
18709565 |
2008 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.
|
18178629 |
2008 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Long-range PCR facilitates the identification of PMS2-specific mutations.
|
16619239 |
2006 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
|
16472587 |
2006 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer.
|
15887124 |
2005 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms.
|
11793469 |
2002 |
|
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.
|
10480359 |
1999 |