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Abstract
Mesh: See more » Chromosome DeletionChromosomes, Human, Pair 22Heart Defects, Congenital/geneticsHeart Defects, Congenital/physiopathologyHumansInfantInfant, NewbornSubclavian Artery/abnormalities
Year: 1999 PMID: 10323529 DOI: 10.1017/s1047951100008532
Source DB: PubMed Journal: Cardiol Young ISSN: 1047-9511 Impact factor: 1.093