rs80338844
|
|
|
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 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs80338844
|
|
|
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 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
|
20065170 |
2010 |
rs80338844
|
|
|
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 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
BEFREE |
A P81L mutation associated with abdominal and head and neck PGL was detected in three families.
|
17102085 |
2006 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
|
15328326 |
2004 |
rs80338844
|
|
|
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 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.
|
11343322 |
2001 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
|
11391798 |
2001 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
|
11391796 |
2001 |
rs80338844
|
|
|
0.720 |
GeneticVariation |
UNIPROT |
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
|
10657297 |
2000 |