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An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 4, p. 337, doi. 10.1111/j.1399-0004.2012.01931.x
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- Publication type:
- Article
Prenatal detection of congenital heart disease--results of a national screening programme.
- Published in:
- 2016
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- Publication type:
- journal article