Congenital knee dislocation in a 49,XXXXY boy.

Por Sijmons, R H, van Essen, A J, Visser, J D, Iprenburg, M, Nelck, G F, Vos-Bender, M L, de Jong, B
Publicado em 1995

Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds

Por Scheenstra, R, Rijcken, F E M, Koornstra, J J, Hollema, H, Fodde, R, Menko, F H, Sijmons, R H, Bijleveld, C M A, Kleibeuker, J H
Publicado em 2003

Geographic clustering of testicular cancer incidence in the northern part of The Netherlands

Por Sonneveld, D J A, Schaapveld, M, Sleijfer, D Th, Meerman, G J Te, Graaf, W T A van der, Sijmons, R H, Koops, H Schraffordt, Hoekstra, H J
Publicado em 1999

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

Por Johansson, L. F., de Boer, E. N., de Weerd, H. A., van Dijk, F., Elferink, M. G., Schuring-Blom, G. H., Suijkerbuijk, R. F., Sinke, R. J., te Meerman, G. J., Sijmons, R. H., Swertz, M. A., Sikkema-Raddatz, B.
Publicado no Sci Rep (2017)

Cost effectiveness of a new strategy to identify HNPCC patients

Por Kievit, W, de Bruin, J H F M, Adang, E M M, Severens, J L, Kleibeuker, J H, Sijmons, R H, Ruers, T J, Nagengast, F M, Vasen, H F A, van Krieken, J H J M, Ligtenberg, M J L, Hoogerbrugge, N
Publicado em 2005

Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

Por Lammens, C. R. M., Bleiker, E. M. A., Aaronson, N. K., Wagner, A., Sijmons, R. H., Ausems, M. G. E. M., Vriends, A. H. J. T., Ruijs, M. W. G., van Os, T. A. M., Spruijt, L., Gómez García, E. B., Cats, A., Nagtegaal, T., Verhoef, S.
Publicado em 2010

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

Por Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Publicado no Fam Cancer (2016)

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non‐polyposis colorectal...

Por Niessen, R C, Berends, M J W, Wu, Y, Sijmons, R H, Hollema, H, Ligtenberg, M J L, de Walle, H E K, de Vries, E G E, Karrenbeld, A, Buys, C H C M, van der Zee, A G J, Hofstra, R M W, Kleibeuker, J H
Publicado em 2006