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J Mogensen

Showing results (51-60 of 57) with videos related to

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Experimental Cell Research|September 1, 1991
Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS)J Mogensen, S Kølvraa, J Hindkjaer, et al.
Heart (British Cardiac Society)|July 16, 2005
Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin IJ C Moon, J Mogensen, P M Elliott, et al.
The Journal of Clinical Investigation|May 20, 1999
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathyJ Mogensen, I C Klausen, A K Pedersen, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Journal of Medical Genetics|January 20, 2004
Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathyJ Mogensen, A Perrot, P S Andersen, et al.
Clinical Genetics|November 10, 2012
Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanismsT B Rasmussen, J Hansen, P H Nissen, et al.
Scientific Reports|April 5, 2020
A Fragment of Collagen Type VI alpha-3 chain is Elevated in Serum from Patients with Gastrointestinal DisordersSigne Holm Nielsen, Joachim Høg Mortensen, Nicholas Willumsen, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Experimental Cell Research|September 1, 1991
Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS)J Mogensen, S Kølvraa, J Hindkjaer, et al.
Heart (British Cardiac Society)|July 16, 2005
Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin IJ C Moon, J Mogensen, P M Elliott, et al.
The Journal of Clinical Investigation|May 20, 1999
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathyJ Mogensen, I C Klausen, A K Pedersen, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Journal of Medical Genetics|January 20, 2004
Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathyJ Mogensen, A Perrot, P S Andersen, et al.
Clinical Genetics|November 10, 2012
Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanismsT B Rasmussen, J Hansen, P H Nissen, et al.
Scientific Reports|April 5, 2020
A Fragment of Collagen Type VI alpha-3 chain is Elevated in Serum from Patients with Gastrointestinal DisordersSigne Holm Nielsen, Joachim Høg Mortensen, Nicholas Willumsen, et al.
Pageof 6