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Browsing by Author Ruijs, M.W.

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Showing results 1 to 4 of 4
Full TextIssue DateTitleAuthor(s)
2011Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromesLammens, C.R.; Bleiker, E.M.; Verhoef, S.; Ausems, M.G.; Majoor-Krakauer, D., et al
2010Genetic 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
2010Regular 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
2010TP53 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
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