Chromosome 22q11 Deletion in Patients with Truncus Arteriosus

Pediatric Cardiology

Volumn 24, Issue 6, 2003, Pages 569-573

  McElhinney, D B ^a,b,c   Driscoll, D A ^a,b   Emanuel, B S ^a,b   Goldmuntz, E ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

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

^c BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

DiGeorge syndrome; Genetics; Velocardiofacial syndrome

Indexed keywords

ANATOMICAL VARIATION; AORTA ARCH; ARTERIAL TRUNK; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; CORRELATION ANALYSIS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PULMONARY ARTERY;

CHI-SQUARE DISTRIBUTION; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; MALE; PHENOTYPE; PROSPECTIVE STUDIES; TRUNCUS ARTERIOSUS, PERSISTENT;

EID: 0345304959     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00246-003-0441-3     Document Type: Article

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