|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Gain of function of mutant p53: R282W on the peak?
|
26878390 |
2016 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
|
26911350 |
2016 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.
|
25619955 |
2015 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Heterogeneity of Li-Fraumeni syndrome links to unequal gain-of-function effects of p53 mutations.
|
24573247 |
2014 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
The TP53 website: an integrative resource centre for the TP53 mutation database and TP53 mutant analysis.
|
23161690 |
2013 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Early onset HER2-positive breast cancer is associated with germline TP53 mutations.
|
21761402 |
2012 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature.
|
22672556 |
2012 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome.
|
21305319 |
2011 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome.
|
21059199 |
2010 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Somatic TP53 mutation mosaicism in a patient with Li-Fraumeni syndrome.
|
19012332 |
2009 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset.
|
19468865 |
2009 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome.
|
11370630 |
2001 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Molecular analysis of the TP53 gene in Barrett's adenocarcinoma.
|
8829627 |
1996 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms.
|
1565144 |
1992 |
|
LI-FRAUMENI SYNDROME 1
|
|
0.700 |
CausalMutation
|
CLINVAR |
Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma.
|
1565143 |
1992 |