×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
9585613 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
9585613 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
9667259 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
Biomarker
CLINGEN
Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells.
9774970 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease.
9537231 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.
9792861 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
9667259 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online.
10660329 1998
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes.
10486320 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Cancer risks in BRCA2 mutation carriers.
10433620 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G.
10595255 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Survival in hereditary breast cancer associated with germline mutations of BRCA2.
10550133 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Truncated BRCA2 is cytoplasmic: implications for cancer-linked mutations.
10570174 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations.
10644434 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
BRCA1/BRCA2 germline mutations in locally recurrent breast cancer patients after lumpectomy and radiation therapy: implications for breast-conserving management in patients with BRCA1/BRCA2 mutations.
10506595 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2.
10188893 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers.
10615237 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study.
10498392 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects.
10227398 1999
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
The BRCA2 genetic variant IVS7 + 2T-->G is a mutation.
11185744 2000
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families.
10638982 2000
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
GeneticVariation
CLINVAR
Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families.
10638982 2000
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
2157delG: a frequent mutation in BRCA2 missed by PTT.
11106360 2000
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the disease.
10978364 2000
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700
CausalMutation
CLINVAR
Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer.
10807692 2000