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7 Most Recent Publications
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High cancer risk and increased mortality in patients with Peutz - Jeghers syndrome
(Article)
Lier, M.G.F. van Westerman, A.M. Wagner, A. Looman, C.W.N. Wilson, J.H.P. Rooij, F.W.M. de Lemmens, V.E.P.P. Kuipers, E.J. Mathus-Vliegen, E.M.H. Leerdam, M.E. van |
2011-02-01
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Novel null-allele mutations and genotype-phenotype correlation in Argentinean patients with erythropoietic protoporphyria
(Article)
Parera, V.E. Koole, R.H. Minderman, G. Edixhoven, A. Rossetti, M.V. Batlle, A. Rooij, F.W.M. de |
2009-11-01
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Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands
(Article)
Rooij, F.W.M. de Kavelaars, F.G. Koole-Lesuis, H. Wilson, J.H.P. |
2009-08-18
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Vitamin D deficiency in patients with erythropoietic protoporphyria
(Article)
Spelt, J.M.C. Rooij, F.W.M. de Wilson, J.H.P. Zandbergen, A.A.M. |
2008-01-01
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Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
(Article)
Leng, W.W.J. de Jansen, M. Giardiello, F.M. Weterman, M.A.J. Offerhaus, G.J.A. Carvalho, R. Polak, M. Musler, A.R. Milne, A.N.A. Keller, J.J. Menko, F. Rooij, F.W.M. de Iacobuzio-Donahue, C.A. |
2007-12-01
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CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies
(Article)
Linde, K. van der Boor, P.P.C. Houwing-Duistermaat, J.J. Crusius, B.J.A. Wilson, P.J.H. Kuipers, E.J. Rooij, F.W.M. de |
2007-06-01
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Nasal polyposis in Peutz-Jeghers syndrome: A distinct histopathological and molecular genetic entity
(Article)
Leng, W.W.J. de Westerman, A.M. Weterman, M.A.J. Jansen, M. Dekken, H. van Giardiello, F.M. Rooij, F.W.M. de Wilson, J.H.P. Offerhaus, G.J.A. Keller, J.J. |
2007-04-01
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