|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Clinical Features, Genetics and Potential Therapeutic Approaches for Birt-Hogg-Dubé Syndrome.
|
26581862 |
2019 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Cutaneous melanoma in Birt-Hogg-Dubé syndrome: part of the clinical spectrum?
|
28869776 |
2018 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Splice-site mutation causing partial retention of intron in the FLCN gene in Birt-Hogg-Dubé syndrome: a case report.
|
29720200 |
2018 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome.
|
28558743 |
2017 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer.
|
28499369 |
2017 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation.
|
27734835 |
2017 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Birt-Hogg-Dube syndrome prospectively detected by review of chest computed tomography scans.
|
28151982 |
2017 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
|
28724667 |
2017 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.
|
26659639 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.
|
27220747 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?
|
26603437 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation.
|
27780965 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types.
|
26402642 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Familial pneumothoraces: Birt-Hogg-Dubé syndrome.
|
27906882 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Birt-Hogg-Dubé Syndrome Presenting as a Nevus Comedonicus-Like Lesion in an 8-Year-Old Boy.
|
27470329 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes.
|
27356891 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
An 18-year-old man with recurrent pneumothorax since he was 10-year-old.
|
27257988 |
2016 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Is cardiac rhabdomyoma a feature of Birt Hogg Dubé syndrome?
|
25655561 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome.
|
25594584 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Possible familial case of Birt-Hogg-Dubé syndrome complicated with lung cancer: A possible link between these two disease entities.
|
26028485 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Genetic analysis of familial spontaneous pneumothorax in an Indian family.
|
25827758 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Perifollicular fibromas associated with Birt-Hogg-Dubé syndrome.
|
26387484 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Birt-Hogg-Dubé syndrome detected incidentally by asymptomatic bilateral pneumothorax in health screening: a case of a young Japanese woman.
|
26943385 |
2015 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patients.
|
24994497 |
2014 |
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
An oncocytic adrenal tumour in a patient with Birt-Hogg-Dubé syndrome.
|
23848572 |
2014 |