rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Multiple endocrine neoplasias type 2B and RET proto-oncogene.
|
22429913 |
2012 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.
|
22429592 |
2012 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.
|
22041710 |
2011 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Update multiple endocrine neoplasia type 2.
|
20087666 |
2010 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Medullary thyroid cancer: management guidelines of the American Thyroid Association.
|
19469690 |
2009 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Hirschsprung disease, associated syndromes and genetics: a review.
|
17965226 |
2008 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Pheochromocytoma penetrance varies by RET mutation in MEN 2A.
|
18063059 |
2007 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Germ-line mutations in nonsyndromic pheochromocytoma.
|
12000816 |
2002 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease.
|
9067749 |
1997 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.
|
8918855 |
1996 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.
|
7906417 |
1994 |
rs1554818540
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.
|
7881414 |
1994 |