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Browsing by Author Ruijs, M.W.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2011 | Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromes | Lammens, C.R.; Bleiker, E.M.; Verhoef, S.; Ausems, M.G.; Majoor-Krakauer, D., 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 |
| 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 |
Showing results 1 to 4 of 4
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