|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes.
|
26888179 |
2016 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Genome sequencing identifies major causes of severe intellectual disability.
|
24896178 |
2014 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Clinical features and genetic analysis of Korean patients with Loeys-Dietz syndrome.
|
22113417 |
2012 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
CTD_human |
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
|
22772368 |
2012 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
CTD_human |
Germline TGF-beta receptor mutations and skeletal fragility: a report on two patients with Loeys-Dietz syndrome.
|
20358619 |
2010 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.
|
19883511 |
2009 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype.
|
18070134 |
2008 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
|
16928994 |
2006 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.
|
16799921 |
2006 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
|
16928994 |
2006 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.
|
16791849 |
2006 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited.
|
16596670 |
2006 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
|
15731757 |
2005 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
|
15731757 |
2005 |
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
7046 |
| Gene Symbol: |
TGFBR1 |
TGFBR1
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|