Global ETD Search
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Showing 1 to 3 of 3 for “"truncus arteriosus"”.
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An analysis of the phenotypic features of chromosomes 22q11.1 deletion syndrome at Red Cross War Memorial Children's Hospital
… isolated VSD (46%), tetralogy of Fallot (20.8%), truncus arteriosus (14.5%), PS/pulmonary artery stenosis (20.8%) and interrupted aortic arch (6%). Interrupted aortic arch was found to be the most sensitive marker for 22qDS in children with cardiac lesions. The cardiac lesions with the highest …
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Anteriore Musterbildung im Wirbeltierembryo - Die Induktion von Vorderhirn und Herz
… Mechanismus bei der Septierung des Trunkus arteriosus sein, dessen Fehlsteuerung zu angeborenen Herzdefekten führt, wie sie beim humanen DiGeorge-Syndrom beobachtet werden.