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Browsing by Author Willems, P.J.
Showing results 1 to 12 of 12
| 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 |
| 2011 | Motor nerve decline does not underlie muscle weakness in type 2 diabetic neuropathy. | Ijzerman, T.H.; Schaper, N.C.; Melai, T.; Blijham, P.J.; Meijer, K., et al |
| 2010 | Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations. | Valstar, M.J.; Bertoli-Avella, A.M.; Wessels, M.W.; Ruijter, G.J.; Graaf, B. 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 |
| 2005 | Autosomal dominant inheritance of left ventricular outflow tract obstruction. | Wessels, M.W.; Berger, R.M.; Frohn-Mulder, I.M.; Roos-Hesselink, J.W.; Hoogeboom, J.J., et al |
| 2004 | Three new families with arterial tortuosity syndrome. | Wessels, M.W.; Catsman-Berrevoets, C.E.; Mancini, G.M.; Breuning, M.H.; Hoogeboom, J.J., et al |
| 1997 | The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q | Coucke, P.; Camp, G. van; Demirhan, O.; Kabakkaya, Y.; Balemans, W., et al |
| 1995 | Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients | Graaff, E. de; Rouillard, P.; Willems, P.J.; Smits, A.P.T.; Rousseau, F., et al |
| 1995 | Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15 | Camp, G. van; Coucke, P.; Balemans, W.; Velzen, D. van; Bilt, C. van de, et al |
| 1995 | Hotspot for Deletions in the Cgg Repeat Region of Fmr1 in Fragile-X Patients | Degraaff, E.; Rouillard, P.; Willems, P.J.; Smits, A.P.T.; Rousseau, F., et al |
| 1976 | Een Romeins grafveld en sporen van prehistorische bewoning aan de Holenbergseweg te Wijchen, 1973 | Haalebos, Jan Kees; Willems, P.J.; Giebels, H.W.L.M. |
Showing results 1 to 12 of 12
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