Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome

American Journal of Cardiology

Volumn 107, Issue 3, 2011, Pages 466-471

  Swaby, Jodi Ann M ^a,b   Silversides, Candice K ^a   Bekeschus, Sean C ^b   Piran, Sara ^a   Oechslin, Erwin N ^a   Chow, Eva W C ^a,b   Bassett, Anne S ^a,b  

^a UNIVERSITY OF TORONTO   (Canada)

^b CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 22; CHROMOSOME DELETION 22Q11; CONGENITAL HEART DISEASE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; DISEASE SEVERITY; FAMILY HISTORY; FEMALE; GENE EXPRESSION; GENETIC COUNSELING; GENETIC RISK; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION GENETICS; PREDICTION; PREVALENCE; PRIORITY JOURNAL; RECURRENCE RISK; RELATIVE;

ADULT; DIGEORGE SYNDROME; FAMILY CHARACTERISTICS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HEART DEFECTS, CONGENITAL; HUMANS; MALE;

EID: 78951482163     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjcard.2010.09.045     Document Type: Article

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