Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
|
25494863 |
2015 |
Pheochromocytoma
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
Pheochromocytoma
|
|
0.800 |
GeneticVariation
|
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
Pheochromocytoma
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Genetic testing in head and neck paraganglioma: who, what, and why?
|
24436918 |
2013 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
|
23433498 |
2013 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
|
21348866 |
2012 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.
|
21937622 |
2011 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas.
|
15479192 |
2004 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
|
11897817 |
2002 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
|
11391796 |
2001 |
Pheochromocytoma
|
|
0.800 |
CausalMutation
|
CLINVAR |
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
|
10657297 |
2000 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
|
25394175 |
2015 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
|
20065170 |
2010 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Endocrine cancer predisposition syndromes: hereditary paraganglioma, multiple endocrine neoplasia type 1, multiple endocrine neoplasia type 2, and hereditary thyroid cancer.
|
20816580 |
2010 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
BEFREE |
A P81L mutation associated with abdominal and head and neck PGL was detected in three families.
|
17102085 |
2006 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
|
15328326 |
2004 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
BEFREE |
P81L and R38X mutations have previously been reported in other PGL families and P81L was suggested as a founder mutation.
|
11897817 |
2002 |
Paraganglioma
|
|
0.720 |
GeneticVariation
|
UNIPROT |
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.
|
11343322 |
2001 |