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Volumn 7, Issue 2, 2012, Pages 145-150

Critical congenital heart disease-utility of routine screening for chromosomal and other extracardiac malformations

Author keywords

Chromosomal defects; Extracardiac malformations; Genetic testing; Head ultrasound; Renal ultrasound

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;

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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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.