Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.
|
19390654 |
2009 |
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
RB1 mutations and second primary malignancies after hereditary retinoblastoma.
|
22205104 |
2012 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Genetic screening in Iranian patients with retinoblastoma.
|
27983729 |
2017 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Targeted next generation sequencing of RB1 gene for the molecular diagnosis of Retinoblastoma.
|
25928201 |
2015 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
RB loss in resistant EGFR mutant lung adenocarcinomas that transform to small-cell lung cancer.
|
25758528 |
2015 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Novel mutations in the RB1 gene from Chinese families with a history of retinoblastoma.
|
25424699 |
2015 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications.
|
11317357 |
2001 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.
|
9400934 |
1997 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis.
|
22963398 |
2013 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
|
15884040 |
2005 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Online.
|
10671068 |
1998 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR.
|
23981928 |
2013 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma.
|
12541220 |
2003 |
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.
|
16269091 |
2005 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
A parent-of-origin effect in two families with retinoblastoma is associated with a distinct splice mutation in the RB1 gene.
|
12016586 |
2002 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.
|
1577465 |
1992 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
|
26396485 |
2015 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
New RB1 oncogenic mutations and intronic polymorphisms in Serbian retinoblastoma patients: genetic counseling implications.
|
16972022 |
2006 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Genetic screening in patients with Retinoblastoma in Israel.
|
25754945 |
2015 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.
|
16269091 |
2005 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer.
|
10966849 |
2000 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Conservation of the RB1 gene in human and primates.
|
15776430 |
2005 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
|
27582626 |
2016 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expression.
|
18181215 |
2008 |
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation
|
group |
CLINVAR |
Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
|
27021801 |
2016 |