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Psychosocial impact of Von Hippel–Lindau disease: levels and sources of distress.
Published in:
Clinical Genetics, 2010, v. 77, n. 5, p. 483, doi. 10.1111/j.1399-0004.2010.01333.x
By:
- Lammens, C. R. M.;
- Bleiker, E. M. A.;
- Verhoef, S.;
- Hes, F. J.;
- Ausems, M. G. E. M.;
- Majoor-Krakauer, D.;
- Sijmons, R. H.;
- van der Luijt, R. B.;
- van den Ouweland, A. M. W.;
- Van Os, Tam;
- Hoogerbrugge, N.;
- García, E. B. Gómez;
- Dommering, C. J.;
- Gundy, C. M.;
- Aaronson, N. K.
Publication type:
Article
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
Published in:
Clinical Genetics, 2007, v. 72, n. 2, p. 122, doi. 10.1111/j.1399-0004.2007.00827.x
By:
- Hes, F. J.;
- van der Luijt, R. B.;
- Janssen, A. L. W.;
- Zewald, R. A.;
- de Jong, G. J.;
- Lenders, J. W.;
- Links, T. P.;
- Luyten, G. P. M.;
- Sijmons, R. H.;
- Eussen, H. J.;
- Halley, D. J. J.;
- Lips, C. J. M.;
- Pearson, P. L.;
- van den Ouweland, A. M. W.;
- Majoor-Krakauer, D. F.
Publication type:
Article
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study.
Published in:
Clinical Genetics, 2007, v. 71, n. 1, p. 35, doi. 10.1111/j.1399-0004.2007.00731.x
By:
- Van Oostrom, I.;
- Meijers-Heijboer, H.;
- Duivenvoorden, H. J.;
- Bröcker-Vriends, A. H. J. T.;
- Van Asperen, C. J.;
- Sijmons, R. H.;
- Seynaeve, C.;
- Van Gool, A. R.;
- Klijn, J. G. M.;
- Tibben, A.
Publication type:
Article
Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.
Published in:
Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2023, v. 30, n. 6, p. 3248, doi. 10.1245/s10434-023-13229-5
By:
- Bokkers, K.;
- Bleiker, E. M. A.;
- Aalfs, C. M.;
- van Dalen, T.;
- Velthuizen, M. E.;
- Duijveman, P.;
- Sijmons, R. H.;
- Koole, W.;
- Schoenmaeckers, E. J. P.;
- Ausems, M. G. E. M.
Publication type:
Article
Prenatal diagnosis in two cases of de novo complex balanced chromosomal rearrangements. Three-year follow-up in one case.
Published in:
1995
By:
- Sikkema-Raddatz, B.;
- Sijmons, R. H.;
- Tan-Sindhunata, M. B.;
- Van Der Veen, A. Y.;
- Brunsting, R.;
- De Vries, B.;
- Beekhuis, J. R.;
- Bekedam, D. J.;
- Van Aken, B.;
- De Jong, B.
Publication type:
journal article
46,XY,dup(10q) in direct CVS preparation and mosaic 48,XXXY,dup(10q) in CVS long-term culture and fetal tissue.
Published in:
1995
By:
- Sijmons, R. H.;
- Sikkema-Raddatz, B.;
- Kloosterman, M. D.;
- Briet, J. W.;
- De Jong, B.;
- Leschot, N. J.
Publication type:
journal article
Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction.
Published in:
1992
By:
- De Boer, Martin;
- Bolscher, Ben G. J. M.;
- Sijmons, Rolf H.;
- Scheffer, Hans;
- Weening, Ron S.;
- Roos, Dirk;
- De Boer, M;
- Bolscher, B G;
- Sijmons, R H;
- Scheffer, H;
- Weening, R S;
- Roos, D
Publication type:
journal article
Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes.
Published in:
Psycho-Oncology, 2011, v. 20, n. 6, p. 631, doi. 10.1002/pon.1951
By:
- Lammens, C. R. M.;
- Bleiker, E. M. A.;
- Verhoef, S.;
- Ausems, M. G. E. M.;
- Majoor‐Krakauer, D.;
- Sijmons, R. H.;
- Hes, F. J.;
- Gómez‐García, E. B.;
- Van Os, T. A. M.;
- Spruijt, L.;
- van der Luijt, R. B.;
- van den Ouweland, A. M. W.;
- Ruijs, M. W. G.;
- Gundy, C.;
- Nagtegaal, T.;
- Aaronson, N. K.
Publication type:
Article
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
Published in:
Familial Cancer, 2016, v. 15, n. 4, p. 563, doi. 10.1007/s10689-016-9877-5
By:
- Ghorbanoghli, Z.;
- Nieuwenhuis, M.;
- Houwing-Duistermaat, J.;
- Jagmohan-Changur, S.;
- Hes, F.;
- Tops, C.;
- Wagner, A.;
- Aalfs, C.;
- Verhoef, S.;
- Gómez García, E.;
- Sijmons, R.;
- Menko, F.;
- Letteboer, T.;
- Hoogerbrugge, N.;
- Wezel, T.;
- Vasen, H.;
- Wijnen, J.
Publication type:
Article
The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome.
Published in:
Familial Cancer, 2013, v. 12, n. 2, p. 175, doi. 10.1007/s10689-013-9616-0
By:
- Plazzer, J.;
- Sijmons, R.;
- Woods, M.;
- Peltomäki, P.;
- Thompson, B.;
- Dunnen, J.;
- Macrae, F.
Publication type:
Article
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review.
Published in:
Familial Cancer, 2013, v. 12, n. 1, p. 43, doi. 10.1007/s10689-012-9570-2
By:
- Knopperts, A.;
- Nielsen, M.;
- Niessen, R.;
- Tops, C.;
- Jorritsma, B.;
- Varkevisser, J.;
- Wijnen, J.;
- Siezen, C.;
- Heine-Bröring, R.;
- Kranen, H.;
- Vos, Y.;
- Westers, H.;
- Kampman, E.;
- Sijmons, R.;
- Hes, F.
Publication type:
Article
Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits.
Published in:
Familial Cancer, 2010, v. 9, n. 4, p. 647, doi. 10.1007/s10689-010-9368-z
By:
- Lammens, C.;
- Bleiker, E.;
- Aaronson, N.;
- Wagner, A.;
- Sijmons, R.;
- Ausems, M.;
- Vriends, A.;
- Ruijs, M.;
- Os, T.;
- Spruijt, L.;
- Gómez García, E.;
- Cats, A.;
- Nagtegaal, T.;
- Verhoef, S.
Publication type:
Article
Geographic clustering of testicular cancer incidence in the northern part of The Netherlands.
Published in:
British Journal of Cancer, 1999, v. 81, n. 7, p. 1262, doi. 10.1038/sj.bjc.6690839
By:
- 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
Publication type:
Article

Found: 13