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Stephan Waldmüller

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Clinical Research in Cardiology : Official Journal of the German Cardiac Society|March 17, 2011
A case of familial hypertrophic cardiomyopathy emphasizes the importance of parallel screening of multiple disease genesThomas Scheffold, Stephan Waldmüller, Konstantin Borisov
Human Mutation|April 23, 2002
Low-density DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathyStephan Waldmüller, Petra Freund, Simon Mauch, et al.
Clinical Chemistry|February 9, 2008
Array-based resequencing assay for mutations causing hypertrophic cardiomyopathyStephan Waldmüller, Melanie Müller, Kirsten Rackebrandt, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|April 10, 2007
Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?Stephan Waldmüller, Melanie Müller, Henning Warnecke, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissectionsSabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
Journal of the American College of Cardiology|May 4, 2019
Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-InhibitionGregor Andelfinger, Christopher Marquis, Marie-Josée Raboisson, et al.
Molecular and Cellular Probes|May 17, 2015
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathiesStephan Waldmüller, Christopher Schroeder, Marc Sturm, et al.
Frontiers in Endocrinology|December 28, 2023
Identification of novel genes including <i>NAV2</i> associated with isolated tall statureBirgit Weiss, Tim Ott, Philipp Vick, et al.
Molecular and Cellular Probes|November 13, 2012
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissectionsUshanthine Kathiravel, Britta Keyser, Sabine Hoffjan, et al.
Brain : a Journal of Neurology|April 18, 2024
Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemiaFelix Distelmaier, Abdullah Sezer, Christina Helm, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|March 17, 2011
A case of familial hypertrophic cardiomyopathy emphasizes the importance of parallel screening of multiple disease genesThomas Scheffold, Stephan Waldmüller, Konstantin Borisov
Human Mutation|April 23, 2002
Low-density DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathyStephan Waldmüller, Petra Freund, Simon Mauch, et al.
Clinical Chemistry|February 9, 2008
Array-based resequencing assay for mutations causing hypertrophic cardiomyopathyStephan Waldmüller, Melanie Müller, Kirsten Rackebrandt, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|April 10, 2007
Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?Stephan Waldmüller, Melanie Müller, Henning Warnecke, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissectionsSabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
Journal of the American College of Cardiology|May 4, 2019
Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-InhibitionGregor Andelfinger, Christopher Marquis, Marie-Josée Raboisson, et al.
Molecular and Cellular Probes|May 17, 2015
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathiesStephan Waldmüller, Christopher Schroeder, Marc Sturm, et al.
Frontiers in Endocrinology|December 28, 2023
Identification of novel genes including <i>NAV2</i> associated with isolated tall statureBirgit Weiss, Tim Ott, Philipp Vick, et al.
Molecular and Cellular Probes|November 13, 2012
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissectionsUshanthine Kathiravel, Britta Keyser, Sabine Hoffjan, et al.
Brain : a Journal of Neurology|April 18, 2024
Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemiaFelix Distelmaier, Abdullah Sezer, Christina Helm, et al.
Pageof 2