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Browsing by Author Graaf, B.M. de
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| Full Text | Issue Date | Title | Author(s) | | 2011 | Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis | Laar, I.M. van de; Oldenburg, R.A.; Pals, G.; Roos-Hesselink, J.W.; Graaf, B.M. de, et al |
| 2009 | Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction. | Wessels, M.W.; Laar, I.M. van de; Roos-Hesselink, J.W.; Strikwerda, S.; Majoor-Krakauer, D.F., et al |
| 2008 | A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p. | Wessels, M.W.; Graaf, B.M. de; Cohen-Overbeek, T.E.; Spitaels, S.E.; Laat, L.E. de Groot-de, et al |
Showing results 1 to 3 of 3
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