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Volumn 7, Issue 2, 2012, Pages 145-150
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Critical congenital heart disease-utility of routine screening for chromosomal and other extracardiac malformations
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Author keywords
Chromosomal defects; Extracardiac malformations; Genetic testing; Head ultrasound; Renal ultrasound
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Indexed keywords
AORTA ARCH ANOMALY;
AORTA COARCTATION;
AORTA VALVE STENOSIS;
AORTOPULMONARY SEPTAL DEFECT;
ARTICLE;
BRAIN MALFORMATION;
CHROMOSOME 22Q11.2 DELETION;
CHROMOSOME ABERRATION;
CHROMOSOME DELETION 22Q11;
CLINICAL PRACTICE;
CONGENITAL HEART DISEASE;
CONGENITAL HEART MALFORMATION;
CONTROLLED STUDY;
DIAGNOSTIC TEST;
DIAGNOSTIC TEST ACCURACY STUDY;
EBSTEIN ANOMALY;
ECHOGRAPHY;
EXTRACARDIAC MALFORMATION;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENETIC SCREENING;
HEAD ULTRASOUND;
HEART;
HEART ATRIUM SEPTUM DEFECT;
HEART SURGERY;
HEART VENTRICLE SEPTUM DEFECT;
HISTOPATHOLOGY;
HOSPITAL ADMISSION;
HUMAN;
INCIDENCE;
INFANT;
INTENSIVE CARE UNIT;
KARYOTYPING;
KIDNEY ANOMALY;
MAJOR CLINICAL STUDY;
MALE;
MEDICAL RECORD REVIEW;
PREMATURITY;
PRIORITY JOURNAL;
PULMONARY VALVE ATRESIA;
PULMONARY VALVE STENOSIS;
PULMONARY VEIN MALFORMATION;
RENAL ECHOGRAPHY;
SCREENING TEST;
TRICUSPID VALVE ATRESIA;
ULTRASOUND;
ABNORMAL KARYOTYPE;
ABNORMALITIES, MULTIPLE;
BRAIN;
CHROMOSOME ABERRATIONS;
COHORT STUDIES;
CRITICAL ILLNESS;
FEMALE;
GENETIC TESTING;
GESTATIONAL AGE;
HEART DEFECTS, CONGENITAL;
HOSPITAL MORTALITY;
HUMANS;
INCIDENCE;
INFANT, NEWBORN;
INTENSIVE CARE UNITS, NEONATAL;
MALE;
MASS SCREENING;
PREVALENCE;
RETROSPECTIVE STUDIES;
RISK FACTORS;
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EID: 84858847952
PISSN: 1747079X
EISSN: 17470803
Source Type: Journal
DOI: 10.1111/j.1747-0803.2011.00585.x Document Type: Article |
Times cited : (31)
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References (8)
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