Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies.

Pediatrics

Volumn 112, Issue 6 Pt 1, 2003, Pages

  McElhinney, Doff B ^a   Driscoll, Deborah A ^a   Levin, Elissa R ^a   Jawad, Abbas F ^a   Emanuel, Beverly S ^a   Goldmuntz, Elizabeth ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 22; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; GENETICS; HEART SEPTUM DEFECT; HUMAN; PHENOTYPE;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; PHENOTYPE;

MLCS; MLOWN;

EID: 0642333838     PISSN: None     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.112.6.e472     Document Type: Article

References (0)