Patient experiences with gene panels based on exome sequencing in clinical diagnostics: high acceptance and low distress von Sie, A.S., Prins, J.B., van Zelst-Stams, W.A.G., Veltman, J.A., Feenstra, I., Hoogerbrugge, N.

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Adding familial risk assessment to faecal occult blood test can increase the effectiveness of population-based colorectal cancer screening von Dekker, N, van Rossum, L.G.M, Van Vugt-van Pinxteren, M, van Stiphout, S.H.C, Hermens, R.P.M.G, van Zelst-Stams, W.A.G, van Oijen, M.G.H, Laheij, R.J.F, Jansen, J.B.M.J, Hoogerbrugge, N

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A novel TP63 mutation in family with ADULT syndrome presenting with eczema and hypothelia von van Zelst-Stams, W.A.G., van Steensel, M.A.M.

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Performance of BRCA1/2 mutation prediction models in male breast cancer patients von Moghadasi, S., Grundeken, V., Janssen, L.A.M., Dijkstra, N.H., Rodríguez‐Girondo, M., van Zelst‐Stams, W.A.G., Oosterwijk, J.C., Ausems, M.G.E.M., Oldenburg, R.A., Adank, M.A., Blom, E.W., Ruijs, M.W.G., van Os, T.A.M., van Deurzen, C.H.M., Martens, J.W.M., Schroder, C.P., Wijnen, J.T., Vreeswijk, M.P.G., van Asperen, C.J.

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Performance of BRCA1/2 mutation prediction models in male breast cancer patients von Moghadasi, S., Grundeken, V., Janssen, L.A.M., Dijkstra, N.H., Rodriguez-Girondo, M., Zelst-Stams, W.A.G. van, Oosterwijk, J.C., Ausems, M.G.E.M., Oldenburg, R.A., Adank, M.A., Blom, E.W., Ruijs, M.W.G., Os, T.A.M. van, Deurzen, C.H.M. van, Martens, J.W.M., Schroder, C.P., Wijnen, J.T., Vreeswijk, M.P.G., Asperen, C.J. van

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Diagnostic exome sequencing in 266 Dutch patients with visual impairment von Haer-Wigman, L., Zelst-Stams, W.A.G. van, Pfundt, R., Born, L.I. van den, Klaver, C.C.W., Verheij, J.B.G.M., Hoyng, C.B., Breuning, M.H., Boon, C.J.F., Kievit, A.J., Verhoeven, V.J.M., Pott, J.W.R., Sallevelt, S.C.E.H., Hagen, J.M. van, Plomp, A.S., Kroes, H.Y., Lelieveld, S.H., Hehir-Kwa, J.Y., Castelein, S., Nelen, M., Scheffer, H., Lugtenberg, D., Cremers, F.P.M., Hoefsloot, L., Yntema, H.G.

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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing von Vogelaar, I.P., Post, R.S. van der, Krieken, J.H.J.M. van, Spruijt, L., Zelst-Stams, W.A.G. van, Kets, C.M., Lubinski, J., Jakubowska, A., Teodorczyk, U., Aalfs, C.M., Hest, L.P. van, Pinheiro, H., Oliveira, C., Jhangiani, S.N., Muzny, D.M., Gibbs, R.A., Lupski, J.R., Ligt, J. de, Vissers, L.E.L.M., Hoischen, A., Gilissen, C., Vorst, M. van de, Goeman, J.J., Schackert, H.K., Ranzani, G.N., Molinaro, V., Garcia, E.B.G., Hes, F.J., Holinski-Feder, E., Genuardi, M., Ausems, M.G.E.M., Sijmons, R.H., Wagner, A., Kolk, L.E. van der, Bjornevoll, I., Hoberg-Vetti, H., Kessel, A.G. van, Kuiper, R.P., Ligtenberg, M.J.L., Hoogerbrugge, N.

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