D B McElhinney, R H Anderson. Show Affiliations »
Abstract
Mesh: See more » Aorta, Thoracic/abnormalitiesChromosome DeletionChromosomes, Human, Pair 22Heart Defects, Congenital/embryologyHeart Defects, Congenital/geneticsHumansVentricular Outflow Obstruction/genetics
Year: 1999 PMID: 10535821 DOI: 10.1017/s1047951100005321
Source DB: PubMed Journal: Cardiol Young ISSN: 1047-9511 Impact factor: 1.093