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- 2024
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Mark
Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young—FGF-21 Highly Associated with Overt Disease
(
- Contribution to journal › Article
- 2023
-
Mark
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions
2023) In European Journal of Human Genetics(
- Contribution to journal › Article
- 2021
-
Mark
High ECG Risk-Scores Predict Late Gadolinium Enhancement on Magnetic Resonance Imaging in HCM in the Young
(
- Contribution to journal › Article
-
Mark
Genetic Variant Score and Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Plakophilin-2 Mutation Carriers
(
- Contribution to journal › Article
- 2020
-
Mark
Hereditary hypertrophic cardiomyopathy in children and young adults—The value of reevaluating and expanding gene panel analyses
(
- Contribution to journal › Article
-
Mark
Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant
(
- Contribution to journal › Article
- 2006
-
Mark
Fluidité, complexité et morphosyntaxe dans la production écrite en FLE
(
- Thesis › Doctoral thesis (monograph)