Implications of genetic testing in noncompaction/hypertrabeculation

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 163, Issue 3, 2013, Pages 206-211

  Shieh, Joseph T C ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cardiomyopathy; Genetic test; Genome; Genomic medicine; Interpretation; Noncompaction; Race; Variant

Indexed keywords

ARTICLE; CARDIOMYOPATHY; CHROMOSOME 1P; CHROMOSOME ABERRATION; CLINICAL LABORATORY; COFFIN LOWRY SYNDROME; COMORBIDITY; CONGENITAL HEART DISEASE; CONSANGUINITY; DE LANGE SYNDROME; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRONIC MEDICAL RECORD; EXOME; FAMILIAL DISEASE; FAMILY HISTORY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE DUPLICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC SCREENING; GENETIC VARIABILITY; GENETICS; GENOME; GENOTYPE; HEARING IMPAIRMENT; HEART ARRHYTHMIA; HEART SURGERY; HIGH THROUGHPUT SEQUENCING; HUMAN; INDEL MUTATION; INHERITANCE; KARYOTYPE; LEOPARD SYNDROME; MARFAN SYNDROME; MICROARRAY ANALYSIS; MYOTONIC DYSTROPHY; NAIL PATELLA SYNDROME; PHENOTYPE; PRIORITY JOURNAL; PSEUDOGENE; SEIZURE; SOTOS SYNDROME; SYMPTOM; TRISOMY 13; TRISOMY 18; VENTRICULAR NONCOMPACTION; CARDIOMYOPATHIES; DNA SEQUENCE; GENETIC PREDISPOSITION; GENOMICS; PATHOPHYSIOLOGY; PROCEDURES;

CARDIOMYOPATHIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; PHENOTYPE; SEQUENCE ANALYSIS, DNA;

EID: 84880702275     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31371     Document Type: Article

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