Oculoectodermal syndrome with coarctation of the aorta and moyamoya disease: Expanding the phenotype to include vascular anomalies
- 18 February 2011
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 155 (3), 577-581
- https://doi.org/10.1002/ajmg.a.33104
Abstract
No abstract availableKeywords
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