Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function.
|
22835832 |
2012 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function.
|
22835832 |
2012 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management.
|
20208144 |
2010 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management.
|
20208144 |
2010 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management.
|
20208144 |
2010 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Chromosomal changes in sporadic and familial head and neck paragangliomas.
|
19393419 |
2009 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
|
18382370 |
2008 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
|
18382370 |
2008 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas.
|
17652212 |
2007 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas.
|
17652212 |
2007 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas.
|
17652212 |
2007 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
|
16317055 |
2006 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.
|
16103922 |
2005 |
PARAGANGLIOMAS 4
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.
|
14500403 |
2003 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.
|
14500403 |
2003 |
Gastrointestinal Stromal Tumors
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.
|
14500403 |
2003 |
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
|
|
|