A new era in clinical genetic testing for hypertrophic cardiomyopathy

Journal of Cardiovascular Translational Research

Volumn 2, Issue 4, 2009, Pages 381-391

  Wheeler, Matthew ^a   Pavlovic, Aleksandra ^a   Degoma, Emil ^a   Salisbury, Heidi ^a   Brown, Colleen ^b   Ashley, Euan A ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Genetic Testing; Hypertrophic Cardiomyopathy; Screening; Sequencing

Indexed keywords

AMYLOIDOSIS; ATHLETE; CLINICAL EVALUATION; CONFIDENTIALITY; DANON DISEASE; DIFFERENTIAL DIAGNOSIS; FABRY DISEASE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GLYCOGEN STORAGE DISEASE TYPE 2; HUMAN; HYPERTENSION; HYPERTROPHIC CARDIOMYOPATHY; LEOPARD SYNDROME; NOONAN SYNDROME; PEDIGREE ANALYSIS; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SARCOMERE; SCORING SYSTEM; SYNDROME DELINEATION; CARDIOMYOPATHY, HYPERTROPHIC; CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL; ECONOMICS; GENETIC MARKER; GENETIC PREDISPOSITION; GENETIC PRIVACY; GENETICS; PREDICTIVE VALUE; PROGNOSIS;

CARDIOMYOPATHY, HYPERTROPHIC; CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC PRIVACY; GENETIC TESTING; HUMANS; PHENOTYPE; PREDICTIVE VALUE OF TESTS; PREIMPLANTATION DIAGNOSIS; PROGNOSIS;

GENETIC MARKER;

EID: 75949105644     PISSN: 19375387     EISSN: 19375395     Source Type: Journal    
DOI: 10.1007/s12265-009-9139-0     Document Type: Review

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