Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.

Pediatrics

Volumn 99, Issue 5, 1997, Pages

  McDonald McGinn, D M ^a   Driscoll, D A ^a   Emanuel, B S ^a   Goldmuntz, E ^a   Clark 3rd , B J ^a   Solot, C ^a   Cohen, M ^a   Schultz, P ^a   LaRossa, D ^a   Randall, P ^a   Zackai, E H ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; CLEFT PALATE; COHORT ANALYSIS; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; EXTERNAL EAR; FACE; GENETICS; HUMAN; INCIDENCE; INFANT; MULTIPLE MALFORMATION SYNDROME; PALATOPHARYNGEAL INCOMPETENCE; PRESCHOOL CHILD; RISK ASSESSMENT;

ABNORMALITIES, MULTIPLE; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLEFT PALATE; COHORT STUDIES; EAR, EXTERNAL; FACE; HEART DEFECTS, CONGENITAL; HUMANS; INCIDENCE; INFANT; RISK ASSESSMENT; VELOPHARYNGEAL INSUFFICIENCY;

MLCS; MLOWN;

EID: 0031130037     PISSN: None     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.99.5.e9     Document Type: Article

References (0)