rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical Features, Genetics and Potential Therapeutic Approaches for Birt-Hogg-Dubé Syndrome.
|
26581862 |
2019 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Cutaneous melanoma in Birt-Hogg-Dubé syndrome: part of the clinical spectrum?
|
28869776 |
2018 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation.
|
27734835 |
2017 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation.
|
27734835 |
2017 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
|
28724667 |
2017 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.
|
27220747 |
2016 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.
|
26659639 |
2016 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.
|
27220747 |
2016 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic analysis of familial spontaneous pneumothorax in an Indian family.
|
25827758 |
2015 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Perifollicular fibromas associated with Birt-Hogg-Dubé syndrome.
|
26387484 |
2015 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Possible familial case of Birt-Hogg-Dubé syndrome complicated with lung cancer: A possible link between these two disease entities.
|
26028485 |
2015 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Birt-Hogg-Dube syndrome is a novel ciliopathy.
|
23784378 |
2013 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
When the chest is clueless, look downstairs.
|
23741947 |
2013 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations.
|
20618353 |
2011 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Choroidal melanoma and lid fibrofoliculomas in Birt-Hogg-Dubé syndrome.
|
21401403 |
2011 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Birt-hogg-dubé syndrome, a rare case in Korea confirmed by genetic analysis.
|
22148048 |
2011 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability.
|
21538689 |
2011 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports.
|
18234728 |
2008 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports.
|
18234728 |
2008 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.
|
17124507 |
2007 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.
|
15852235 |
2005 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Clinical and genetic studies of Birt-Hogg-Dubé syndrome.
|
12471204 |
2002 |
rs80338682
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical and genetic studies of Birt-Hogg-Dubé syndrome.
|
12471204 |
2002 |
rs80338682
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome.
|
12204536 |
2002 |