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Browsing by Author Laar, I.M. van de
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2012 | NPHP4 variants are associated with pleiotropic heart malformations. | French, V.M.; Laar, I.M. van de; Wessels, M.W.; Rohe, C.; Roos-Hesselink, J.W., et al |
| 2012 | Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants. | Linde, D. van der; Laar, I.M. van de; Bertoli-Avella, A.M.; Oldenburg, R.A.; Bekkers, J.A., et al |
| 2012 | Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome. | Laar, I.M. van de; Linde, D. van der; Oei, E.H.; Bos, P.K.; Bessems, J.H., et al |
| 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 |
Showing results 1 to 5 of 5
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