Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations.
|
27144938 |
2016 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations.
|
27144938 |
2016 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
A Novel Mutation in THRA Gene Associated With an Atypical Phenotype of Resistance to Thyroid Hormone.
|
26037512 |
2015 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
A Novel Mutation in THRA Gene Associated With an Atypical Phenotype of Resistance to Thyroid Hormone.
|
26037512 |
2015 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Thyroid hormone resistance syndrome due to mutations in the thyroid hormone receptor α gene (THRA).
|
25670821 |
2015 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Thyroid hormone resistance syndrome due to mutations in the thyroid hormone receptor α gene (THRA).
|
25670821 |
2015 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients.
|
24969835 |
2014 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients.
|
24969835 |
2014 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
An adult female with resistance to thyroid hormone mediated by defective thyroid hormone receptor α.
|
23940126 |
2013 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
An adult female with resistance to thyroid hormone mediated by defective thyroid hormone receptor α.
|
23940126 |
2013 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Clinical phenotype of a new type of thyroid hormone resistance caused by a mutation of the TRα1 receptor: consequences of LT4 treatment.
|
23633213 |
2013 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Clinical phenotype of a new type of thyroid hormone resistance caused by a mutation of the TRα1 receptor: consequences of LT4 treatment.
|
23633213 |
2013 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
A mutation in the thyroid hormone receptor alpha gene.
|
22168587 |
2012 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
|
22604720 |
2012 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Clinical phenotype and mutant TRα1.
|
22494134 |
2012 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
A mutation in the thyroid hormone receptor alpha gene.
|
22168587 |
2012 |
Dysmorphic features
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
Clinical phenotype and mutant TRα1.
|
22494134 |
2012 |
Dysmorphic features
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
|
22604720 |
2012 |