Frequency of 22q11 deletions in patients with conotruncal defects

Journal of the American College of Cardiology

Volumn 32, Issue 2, 1998, Pages 492-498

  Goldmuntz, Elizabeth ^a,b   Clark, Bernard J ^a,b   Mitchell, Laura E ^a,b   Jawad, Abbas F ^a,b   Cuneo, Bettina F ^c   Reed, Lori ^a   McDonald Mcginn, Donna ^a   Chien, Peggy ^a   Feuer, Jennifer ^a   Zackai, Elaine H ^a,b   Emanuel, Beverly S ^a,b   Driscoll, Deborah A ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

^c ADVOCATE CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA ARCH INTERRUPTION; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL HEART DISEASE; DIGEORGE SYNDROME; FALLOT TETRALOGY; FEMALE; GREAT VESSELS TRANSPOSITION; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART VENTRICLE SEPTUM DEFECT; HUMAN; MAJOR CLINICAL STUDY; MALE; PATENT DUCTUS ARTERIOSUS; PRIORITY JOURNAL; VELOCARDIOFACIAL SYNDROME;

AORTA, THORACIC; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DOUBLE OUTLET RIGHT VENTRICLE; FACE; FEMALE; GENETIC SCREENING; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INCIDENCE; MALE; PROSPECTIVE STUDIES; PULMONARY ARTERY; SYNDROME; TETRALOGY OF FALLOT; TRANSPOSITION OF GREAT VESSELS; TRUNCUS ARTERIOSUS, PERSISTENT;

EID: 17444434198     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0735-1097(98)00259-9     Document Type: Article

References (24)

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