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Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2017, Volume 91, Issue 1, pp. 22 - 29
A phenotype‐driven approach to molecular autopsy based in a multidisciplinary team comprising clinical and laboratory genetics, forensic medicine and... 
sudden death | clinical phenotyping | genetic testing | molecular autopsy | UNEXPLAINED DEATH | LONG-QT SYNDROME | RIGHT-VENTRICULAR CARDIOMYOPATHY/DYSPLASIA | FAMILIAL DILATED CARDIOMYOPATHY | HYPERTROPHIC CARDIOMYOPATHY | YOUNG | GENETIC ISSUES | GENETICS & HEREDITY | MUTATIONS | SPECTRUM | CHANNELOPATHIES | Channelopathies - complications | Humans | Middle Aged | Child, Preschool | Infant | Male | Cardiomyopathy, Hypertrophic - complications | Death, Sudden, Cardiac - etiology | Arrhythmogenic Right Ventricular Dysplasia - diagnosis | Arrhythmogenic Right Ventricular Dysplasia - genetics | Young Adult | Cardiomyopathies - genetics | Channelopathies - diagnosis | Cardiomyopathies - diagnosis | Pathology, Molecular - methods | Adult | Cardiomyopathy, Dilated - diagnosis | Female | Child | Cardiomyopathy, Dilated - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease - genetics | Cardiomyopathy, Dilated - complications | Autopsy - methods | Cardiomyopathy, Hypertrophic - diagnosis | Arrhythmogenic Right Ventricular Dysplasia - complications | Channelopathies - genetics | Phenotype | Adolescent | Death, Sudden, Cardiac - pathology | Cardiomyopathies - complications | Aged | Mutation | Heart | Genetic aspects | Cardiac arrest | Genotype & phenotype | Cardiovascular disease | Autopsies | Cardiomyopathy
Journal Article
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2016, Volume 22, Issue 12, pp. 1470 - 1474
Journal Article
NATURE REVIEWS CANCER, ISSN 1474-175X, 12/2019, Volume 19, Issue 12, pp. 686 - 697
Journal Article