Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
|
25645574 |
2015 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
|
25711197 |
2015 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
|
25452455 |
2015 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
|
25394175 |
2015 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
|
24310308 |
2014 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
|
25003300 |
2014 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
|
25070057 |
2014 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
|
23408351 |
2013 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
|
23535968 |
2013 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.
|
22167527 |
2012 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.
|
22102614 |
2012 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants.
|
21120944 |
2011 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
|
20065170 |
2010 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.
|
18561205 |
2008 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Functional analysis of HNPCC-related missense mutations in MSH2.
|
18822302 |
2008 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.
|
18781619 |
2008 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study).
|
16451135 |
2006 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
|
15870828 |
2005 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.
|
15896463 |
2005 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
|
15046096 |
2004 |
Colorectal cancer, hereditary nonpolyposis, type 1
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.
|
12658575 |
2003 |