Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries

Heart

Volumn 79, Issue 2, 1998, Pages 180-185

  Hofbeck, Michael ^a   Rauch, Anita ^b   Buheitel, Gernot ^a   Leipold, Georg ^a   Von Der Emde, Jürgen ^b   Pfeiffer, Rudolf ^b   Singer, Helmut ^a  

^a UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

CATCH 22; Conotruncal anomaly face syndrome; Major aortopulmonary collateral arteries; Pulmonary atresia and ventricular septal defect

Indexed keywords

ADOLESCENT; ADULT; AORTOPULMONARY SEPTAL DEFECT; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COLLATERAL CIRCULATION; CONGENITAL HEART MALFORMATION; CYTOGENETICS; FACE MALFORMATION; FEMALE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; LUNG ATRESIA; MALE; MONOSOMY; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL;

EID: 0031920159     PISSN: 13556037     EISSN: None     Source Type: Journal    
DOI: 10.1136/hrt.79.2.180     Document Type: Article

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