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Browsing by Author Wagner, A.

Full Text	Issue Date	Title	Author(s)
	2012	Risks of less common cancers in proven mutation carriers with lynch syndrome	Engel, C.; Loeffler, M.; Steinke, V.; Rahner, N.; Holinski-Feder, E., et al
	2010	Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients.	Klift, H.M. van der; Tops, C.M.; Bik, E.C.; Boogaard, M.W.; Borgstein, A.M., et al
	2010	TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.	Ruijs, M.W.; Verhoef, S.; Rookus, M.A.; Pruntel, R.; Hout, A.H. van der, et al
	2010	Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats.	You, J.F.; Buhard, O.; Ligtenberg, M.J.L.; Kets, C.M.; Niessen, R.C., et al
	2010	Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.	Lammens, C.R.; Aaronson, N.K.; Wagner, A.; Sijmons, R.H.; Ausems, M.G.E.M., et al
	2010	Regular surveillance for Li-Fraumeni Syndrome: advice, adherence and perceived benefits.	Lammens, C.R.; Bleiker, E.M.A.; Aaronson, N.K.; Wagner, A.; Sijmons, R.H., et al
	2009	Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.	Wijnen, J.T.; Brohet, R.M.; Eijk, R. van; Jagmohan-Changur, S.; Middeldorp, A., et al
	2009	Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndrome.	Lier, M.G. Van; Wilt, J.H.W. de; Wagemakers, J.J.; Dinjens, W.N.; Damhuis, R.A., et al
	2009	Attitude towards pre-implantation genetic diagnosis for hereditary cancer.	Lammens, C.; Bleiker, E.M.A.; Aaronson, N.K.; Vriends, A.H.; Ausems, M.G.E.M., et al
	2008	Identification of phonemes: Differences between phoneme classes and the effect of class size	Wagner, A.; Ernestus, M.T.C.
	2005	Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).	Nielsen, M.; Franken, P.F.; Reinards, T.H.; Weiss, M.M.; Wagner, A., et al
	2004	Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.	Klevering, B.J.; Maugeri, A.; Wagner, A.; Go, S.L.; Vink, C.W., et al
	2004	Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy.	Seynaeve, C.; Verhoog, L.C.; Bosch, L.M. van de; Geel, A.N. van; Menke-Pluymers, M., et al
	2004	Language-specific relevance of formant transitions for fricative	Wagner, A.; Ernestus, M.T.C.