Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart disease

International Journal of Cardiology

Volumn 131, Issue 1, 2008, Pages 51-58

  Fung, Wai Lun Alan ^a,b   Chow, Eva W C ^a,b   Webb, Gary D ^c,d   Gatzoulis, Michael A ^c,e   Bassett, Anne S ^a,b,c  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY HEALTH NETWORK   (Canada)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e ROYAL BROMPTON HOSPITAL   (United Kingdom)

Author keywords

22q11.2 Deletion Syndrome; Adult congenital heart disease; DiGeorge syndrome; Discriminant ability; Genetics; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ADULT; AORTA ARCH; ARTICLE; CHROMOSOME 22Q; CHROMOSOME 22Q11.2; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART DISEASE; DEMOGRAPHY; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; FACE DYSMORPHIA; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HEART SURGERY; HUMAN; LARYNX DISORDER; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; NASAL SPEECH; OUTPATIENT DEPARTMENT; PHYSICIAN; PREDICTION; PRIORITY JOURNAL; RISK; SCREENING;

ADOLESCENT; ADULT; AGE FACTORS; CRANIOFACIAL ABNORMALITIES; DIGEORGE SYNDROME; FEMALE; GENETIC SCREENING; HEART DEFECTS, CONGENITAL; HUMANS; MALE; MIDDLE AGED; PREDICTIVE VALUE OF TESTS; YOUNG ADULT;

EID: 56349136292     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2007.08.141     Document Type: Article

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