Congenital heart disease and aneuploidy

Prenatal Diagnosis

Volumn 24, Issue 13, 2004, Pages 1116-1122

  Wimalasundera, R C ^a   Gardiner, H M ^a,b  

^a QUEEN CHARLOTTE S AND CHELSEA HOSPITAL   (United Kingdom)

^b IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

22q11; Aneuploidy; Congenital heart disease; Karyotype; Trisomy 21

Indexed keywords

ABSENT PULMONARY VALVE SYNDROME; ANEUPLOIDY; AORTA COARCTATION; ARTERIAL TRUNK; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CONGENITAL HEART DISEASE; DISEASE ASSOCIATION; FALLOT TETRALOGY; FETUS; GENETIC COUNSELING; GREAT VESSELS TRANSPOSITION; HEART ATRIUM SEPTUM DEFECT; HEART DOUBLE INLET VENTRICLE; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART SINGLE VENTRICLE; HEART VENTRICLE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; KARYOTYPE; LUNG ATRESIA; PARENT COUNSELING; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROGNOSIS; PULMONARY VALVE DISEASE; PULMONARY VALVE STENOSIS; REVIEW; TRICUSPID VALVE DISEASE; TRISOMY 13; TRISOMY 18; TRISOMY 21; TURNER SYNDROME;

ANEUPLOIDY; FEMALE; GENETIC COUNSELING; HEART DEFECTS, CONGENITAL; HUMANS; INCIDENCE; MASS SCREENING; PATIENT CARE TEAM; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 11144222592     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1068     Document Type: Review

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