The rare association of tetralogy of Fallot with hypertrophic cardiomyopathy: Report of 2 neonatal patients

Texas Heart Institute Journal

Volumn 24, Issue 3, 1997, Pages 215-217

  Lewin, Mark B ^a   Towbin, Jeffrey A ^a   Thapar, Mohinder K ^b   Dreyer, William J ^a   Feltes, Timothy F ^a  

^a TEXAS CHILDREN S HOSPITAL   (United States)

^b UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

Cardiac genetics; Cardiomyopathy, hypertrophic genetics; Chromosome abnormalities genetics; Congenital; Heart defects; Pediatric cardiology; Tetralogy of Fallot

Indexed keywords

ARTICLE; AUTOSOME ABERRATION; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DISEASE ASSOCIATION; FALLOT TETRALOGY; GENE LOCATION; GENE MAPPING; GENETIC ANALYSIS; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INFANT; MALE;

CARDIOMYOPATHY, HYPERTROPHIC; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 1; FATAL OUTCOME; FOLLOW-UP STUDIES; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; RISK FACTORS; TETRALOGY OF FALLOT;

EID: 0030772673     PISSN: 07302347     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

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