Predicting 22q11.2 deletion syndrome: A novel method using the routine full blood count

International Journal of Cardiology

Volumn 150, Issue 1, 2011, Pages 50-53

  Naqvi, N ^a   Davidson, S J ^a   Wong, D ^a   Cullinan, P ^b   Roughton, M ^a   Doughty, V L ^a   Franklin, R C G ^a   Daubeney, P E F ^a,b  

^a ROYAL BROMPTON HOSPITAL   (United Kingdom)

^b NATIONAL HEART AND LUNG INSTITUTE   (United Kingdom)

Author keywords

22q11.2; Congenital heart disease; DiGeorge; Paediatric; Platelet

Indexed keywords

ADOLESCENT; ARTICLE; BLOOD CELL COUNT; CASE CONTROL STUDY; CHROMOSOME DELETION 22Q11; COHORT ANALYSIS; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FEMALE; HEART SURGERY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; PREDICTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SCREENING TEST; THROMBOCYTE VOLUME;

BLOOD CELL COUNT; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 22; COHORT STUDIES; DIGEORGE SYNDROME; FEMALE; HUMANS; INFANT, NEWBORN; MALE; PREDICTIVE VALUE OF TESTS; RETROSPECTIVE STUDIES;

EID: 79960061714     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2010.02.027     Document Type: Article

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