|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
|
17200671 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
|
17200671 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women.
|
18053174 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Analysis of PALB2/FANCN-associated breast cancer families.
|
17420451 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
|
17200672 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
|
17200668 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
A recurrent mutation in PALB2 in Finnish cancer families.
|
17287723 |
2007 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Penetrance analysis of the PALB2 c.1592delT founder mutation.
|
18628482 |
2008 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype.
|
19383810 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Structural basis for recruitment of BRCA2 by PALB2.
|
19609323 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families.
|
18302019 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.
|
18446436 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
|
19264984 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Structural basis for recruitment of BRCA2 by PALB2.
|
19609323 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
|
19264984 |
2009 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
A novel germline PALB2 deletion in Polish breast and ovarian cancer patients.
|
20122277 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
PALB2: a novel inactivating mutation in a Italian breast cancer family.
|
20852946 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
A PALB2 mutation associated with high risk of breast cancer.
|
21182766 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Cooperation of breast cancer proteins PALB2 and piccolo BRCA2 in stimulating homologous recombination.
|
20871615 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
PALB2 mutations in European familial pancreatic cancer families.
|
20412113 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
A PALB2 germline mutation associated with hereditary breast cancer in Italy.
|
19763884 |
2010 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.
|
21285249 |
2011 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
|
21618343 |
2011 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
PALB2 mutations in German and Russian patients with bilateral breast cancer.
|
21165770 |
2011 |
|
| Entrez Id: |
79728 |
| Gene Symbol: |
PALB2 |
PALB2
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer.
|
21618343 |
2011 |