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Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.
Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly.
Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?
Genetic disorders of cardiac morphogenesis. The DiGeorge and velocardiofacial syndromes.
[A successful surgical case of supravalvular aortic stenosis with Williams syndrome: the investigations of the procedures].