|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers.
|
8764110 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
GeneticVariation |
CLINVAR |
BRCA1 mutations in a population-based sample of young women with breast cancer.
|
8531967 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. UKCCCR Familial Ovarian Cancer Study Group.
|
8644703 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.
|
8644702 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core.
|
8807330 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds.
|
8651293 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
New Austrian mutation in BRCA1 gene detected in three unrelated HBOC families.
|
8622478 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.
|
8554067 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites.
|
8933332 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Identification of seven new BRCA1 germline mutations in Italian breast and breast/ovarian cancer families.
|
8968102 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations.
|
8875986 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
BRCA1 mutations in German breast-cancer families.
|
8900426 |
1996 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?
|
9042907 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families.
|
9115959 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
GeneticVariation |
CLINVAR |
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
|
9333265 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.
|
9150149 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Mutational analysis of BRCA1 gene in ovarian and breast-ovarian cancer families in Japan.
|
9197534 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
|
9333265 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes.
|
9361038 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.
|
9150154 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families.
|
9391879 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
|
9150171 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
GeneticVariation |
CLINVAR |
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.
|
9354803 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families.
|
9150151 |
1997 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
Neoplastic Syndromes, Hereditary
|
0.150 |
CausalMutation |
CLINVAR |
A screening for BRCA1 mutations in breast and breast-ovarian cancer families from the Stockholm region.
|
9192828 |
1997 |