|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
|
27082122 |
2016 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
|
25524337 |
2014 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
|
25714468 |
2014 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics.
|
23785128 |
2013 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy.
|
23674513 |
2013 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.
|
23283745 |
2013 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells.
|
23290139 |
2013 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.
|
23233322 |
2013 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
A novel cardiac myosin-binding protein C S297X mutation in hypertrophic cardiomyopathy.
|
20350521 |
2010 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.
|
18533079 |
2008 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Worse prognosis with gene mutations of beta-myosin heavy chain than myosin-binding protein C in Chinese patients with hypertrophic cardiomyopathy.
|
18383048 |
2008 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Mutations profile in Chinese patients with hypertrophic cardiomyopathy.
|
15563892 |
2005 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease.
|
15858117 |
2005 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.
|
15358028 |
2004 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
|
12707239 |
2003 |
|
Hypertrophic Cardiomyopathy
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.
|
10750581 |
1999 |