Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling.
|
28575107 |
2017 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
|
27582626 |
2016 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
|
27582626 |
2016 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline Mutations in Predisposition Genes in Pediatric Cancer.
|
26580448 |
2015 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Genetic screening in patients with Retinoblastoma in Israel.
|
25754945 |
2015 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
RB loss in resistant EGFR mutant lung adenocarcinomas that transform to small-cell lung cancer.
|
25758528 |
2015 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening of RB1 gene mutations in Chinese patients with retinoblastoma and preliminary exploration of genotype-phenotype correlations.
|
24791139 |
2014 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening of RB1 gene mutations in Chinese patients with retinoblastoma and preliminary exploration of genotype-phenotype correlations.
|
24791139 |
2014 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients.
|
24688104 |
2014 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis.
|
22963398 |
2013 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Phenotypic variability of retinocytomas: preregression and postregression growth patterns.
|
22328814 |
2012 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Ten novel RB1 gene mutations in patients with retinoblastoma.
|
17960112 |
2007 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma.
|
12541220 |
2003 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.
|
2594029 |
1989 |
Retinoblastoma
|
|
0.700 |
CausalMutation
|
CLINVAR |
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.
|
2594029 |
1989 |