×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
The clinical spectrum of RET proto-oncogene mutations in codon 790.
23756355 2013
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Novel tandem germline RET proto-oncogene mutations in a patient with multiple endocrine neoplasia type 2B: report of a case and a literature review of tandem RET mutations with in silico analysis.
23468374 2013
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Mutation screening in a Norwegian cohort with pheochromocytoma.
23407919 2013
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A.
23617071 2013
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Patients with RET D631Y mutations most commonly present with pheochromocytoma and not medullary thyroid carcinoma.
22274720 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma.
22068382 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden.
22270996 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene.
22403753 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Failure of pentagastrin-stimulated calcitonin testing in early manifestation of familial medullary thyroid cancer.
22965292 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Hirschsprung's disease and medullary thyroid carcinoma: 15-year experience with molecular genetic screening of the RET proto-oncogene.
21986619 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Role of prophylactic thyroidectomy in RET 790 familial medullary thyroid carcinoma.
21688339 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China.
23210566 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma.
21765987 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family.
21678021 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
21690267 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
RET germline mutations predispose to the development of inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN2).21422799 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Indolent medullary thyroid cancer with a RET proto-oncogene Cys618Phe mutation presenting as sporadic unilateral pheochromocytoma in a 55-year-old Korean woman.
21254918 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.
21810974 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10.
20979234 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Germline RET sequence variation I852M and occult medullary thyroid cancer: harmless polymorphism or causative mutation?
21711375 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene.
21479187 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
"Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 ""Janus"" genetic variation."
20152359 2010
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
A Korean family of familial medullary thyroid cancer with Cys618Ser RET germline mutation.
20119574 2010
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro.
20103606 2010
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Update multiple endocrine neoplasia type 2.
20087666 2010