|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
The RASopathies.
|
23875798 |
2013 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
The RASopathies.
|
23875798 |
2013 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
|
19206169 |
2009 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
|
19206169 |
2009 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.
|
18413255 |
2008 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome.
|
18413255 |
2008 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Neurological complications of cardio-facio-cutaneous syndrome.
|
18039235 |
2007 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Neurological complications of cardio-facio-cutaneous syndrome.
|
18039235 |
2007 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
The cardiofaciocutaneous syndrome.
|
16825433 |
2006 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
LEOPARD syndrome: clinical diagnosis in the first year of life.
|
16523510 |
2006 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
LEOPARD syndrome: clinical diagnosis in the first year of life.
|
16523510 |
2006 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
The cardiofaciocutaneous syndrome.
|
16825433 |
2006 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Multiple lentigenes syndrome.
|
5771505 |
1969 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Multiple lentigenes syndrome.
|
5771505 |
1969 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.
|
4386970 |
1968 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.
|
4386970 |
1968 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|