rs200844292
|
|
|
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 |
rs200844292
|
|
|
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 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
|
15604628 |
2004 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
|
11524739 |
2001 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
RB1 gene mutations in peripheral blood DNA of patients with isolated unilateral retinoblastoma.
|
9973307 |
1999 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Online.
|
10671068 |
1998 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
|
9311732 |
1997 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genetics of retinoblastoma: a study.
|
9140452 |
1997 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene.
|
8776589 |
1996 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Germline mutations in the RB1 gene in patients with hereditary retinoblastoma.
|
8605116 |
1995 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma.
|
7795591 |
1995 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.
|
7927327 |
1994 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.
|
7704558 |
1994 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma.
|
8346255 |
1993 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.
|
1352883 |
1992 |
rs200844292
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.
|
2594029 |
1989 |