|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
|
25525159 |
2015 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mitochondrial variants in MT-CO2 and D-loop instability are involved in MUTYH-associated polyposis.
|
26138249 |
2015 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
|
20685668 |
2010 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
|
20685668 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.
|
18433509 |
2008 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
|
17411426 |
2007 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
|
17411426 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
|
17411426 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
APC germ-line mutations in southern Spanish patients with familial adenomatous polyposis: genotype-phenotype correlations and identification of eight novel mutations.
|
15857185 |
2005 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
APC germ-line mutations in southern Spanish patients with familial adenomatous polyposis: genotype-phenotype correlations and identification of eight novel mutations.
|
15857185 |
2005 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations.
|
15024739 |
2004 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.
|
10094547 |
1999 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.
|
10094547 |
1999 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.
|
1316610 |
1992 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.
|
1316610 |
1992 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.
|
1316610 |
1992 |
|
Desmoid disease, hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
|
Colorectal Carcinoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
|
Stomach Neoplasms
|
|
0.700 |
CausalMutation
|
CLINVAR |
|
|
|