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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
Smit, D. L., Mensenkamp, A. R., Badeloe, S., Breuning, M. H., Simon, M. E. H., van Spaendonck, K. Y., Aalfs, C. M., Post, J. G., Shanley, S., Krapels, I. P. C., Hoefsloot, L. H., van Moorselaar, R. J. A., Starink, T. M., Bayley, J.-P., Frank, J., van Steensel, M. A. M. & Menko, F. H., 2011, In: Clinical genetics. 79, 1, p. 49-59Research output: Contribution to journal › Article* › Academic › peer-review
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Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
Houweling, A. C., Gijezen, L. M., Jonker, M. A., van Doorn, M. B. A., Oldenburg, R. A., van Spaendonck-Zwarts, K. Y., Leter, E. M., van Os, T. A., van Grieken, N. C. T., Jaspars, E. H., de Jong, M. M., Bongers, E. M. H. F., Johannesma, P. C., Postmus, P. E., van Moorselaar, R. J. A., van Waesberghe, J.-H. T. M., Starink, T. M., van Steensel, M. A. M., Gille, J. J. P. & Menko, F. H., 2011, In: British journal of cancer. 105, 12, p. 1912-1919Research output: Contribution to journal › Article* › Academic › peer-review
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Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families
Leter, E. M., Koopmans, A. K., Gille, J. J. P., van Os, T. A. M., Vittoz, G. G., David, E. F. L., Jaspars, E. H., Postmus, P. E., van Moorselaar, R. J. A., Craanen, M. E., Starink, T. M. & Menko, F. H., 2008, In: Journal of investigative dermatology. 128, 1, p. 45-49Research output: Contribution to journal › Article* › Academic › peer-review
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