rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Genetic testing in pheochromocytoma or functional paraganglioma.
|
16314641 |
2005 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
|
18382370 |
2008 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Genetics of pheochromocytoma and paraganglioma in Spanish patients.
|
19258401 |
2009 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
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 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma.
|
20592014 |
2010 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Hereditary paraganglioma of the nasopharynx.
|
20614293 |
2008 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer.
|
23083876 |
2012 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.
|
23934599 |
2014 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes.
|
24509376 |
2014 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography.
|
25791839 |
2015 |
rs587782604
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling.
|
27604842 |
2017 |