Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Three novel mutations in the RET proto-oncogene.
|
11692159 |
2001 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A RET double mutation in the germline of a kindred with FMTC.
|
10826520 |
2000 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma.
|
10323403 |
1999 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma.
|
9677065 |
1998 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma.
|
9621513 |
1998 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.
|
9506724 |
1998 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma.
|
9452077 |
1998 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma.
|
9398735 |
1997 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting.
|
9259198 |
1997 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC.
|
9223675 |
1997 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations.
|
8807338 |
1996 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.
|
8557249 |
1996 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC.
|
7845675 |
1995 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas.
|
8625130 |
1995 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
RET mutations in exons 13 and 14 of FMTC patients.
|
7784092 |
1995 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
RET proto-oncogene mutations in French MEN 2A and FMTC families.
|
7874109 |
1994 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.
|
7881414 |
1994 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests.
|
7915165 |
1994 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer.
|
7849720 |
1994 |
Familial medullary thyroid carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.
|
8103403 |
1993 |