22q11 deletions in patients with conotruncal heart defects

Journal of Paediatrics and Child Health

Volumn 34, Issue 5, 1998, Pages 438-443

  Worthington, S ^a,d   Bower, C ^b   Harrop, K ^a   Loh, J ^c   Walpole, I ^a  

^a PRINCESS MARGARET HOSPITAL FOR CHILDREN   (Australia)

^b Birth Defects Registry W Australia   (Australia)

^c KING EDWARD MEMORIAL HOSPITAL   (Australia)

^d SYDNEY CHILDREN'S HOSPITAL   (Australia)

Author keywords

22q11 deletion; Conotruncal heart defect; Velo cardio facial syndrome

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FAMILY HISTORY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; FEMALE; GENETIC SCREENING; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; PEDIGREE; PREVALENCE; RISK FACTORS;

EID: 0031758081     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1754.1998.00262.x     Document Type: Article

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