Cancer risks in BRCA2 families: estimates for sites other than breast and ovary von van Asperen, C J, Brohet, R M, Meijers-Heijboer, E J, Hoogerbrugge, N, Verhoef, S, Vasen, H F A, Ausems, M G E M, Menko, F H, Gomez Garcia, E B, Klijn, J G M, Hogervorst, F B L, van Houwelingen, J C, van’t Veer, L J, Rookus, M A, van Leeuwen, F E

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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis von Smit, DL, Mensenkamp, AR, Badeloe, S, Breuning, MH, Simon, MEH, Van Spaendonck, KY, Aalfs, CM, Post, JG, Shanley, S, Krapels, IPC, Hoefsloot, LH, Van Moorselaar, RJA, Starink, TM, Bayley, J-P, Frank, J, Van Steensel, MAM, Menko, FH

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MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families von VASEN, H. F. A, STORMORKEN, A, MENKO, F. H, NAGENGAST, F. M, KLEIBEUKER, J. H, GRIFFIOEN, G, TAAL, B. G, MOLLER, P, WIJNEN, J. T

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Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D) von Vasen, H F A, Ghorbanoghli, Z, Bourdeaut, F, Cabaret, O, Caron, O, Duval, A, Entz-Werle, N, Goldberg, Y, Ilencikova, D, Kratz, C P, Lavoine, N, Loeffen, J, Menko, F H, Muleris, M, Sebille, G, Colas, C, Burkhardt, B, Brugieres, L, Wimmer, K

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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 von 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-Htm, Starink, T M, van Steensel, M A M, Gille, J J P, Menko, F H

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Metastatic disease after removal of a renal cell carcinoma smaller than 3 cm in a patient with Birt-Hogg-Dubé syndrome, a case report von van Riel, L., Kets, C. M., van Hest, L. P., Menko, F. H., Boerrigter, B. G., Franken, S. M., Wolthuis, R. M.F., Dubbink, H. J., Zondervan, P. J., van Moorselaar, R. J.A., Houweling, A. C., van de Beek, I.

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Absence of the Birt-Hogg-Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility von Preston, R S, Philp, A, Claessens, T, Gijezen, L, Dydensborg, A B, Dunlop, E A, Harper, K T, Brinkhuizen, T, Menko, F H, Davies, D M, Land, S C, Pause, A, Baar, K, van Steensel, M A M, Tee, A R

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Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP) von Nielsen, M, Franken, P F, Reinards, T H C M, Weiss, M M, Wagner, A, van der Klift, H, Kloosterman, S, Houwing-Duistermaat, J J, Aalfs, C M, Ausems, M G E M, Bröcker-Vriends, A H J T, Gomez Garcia, E B, Hoogerbrugge, N, Menko, F H, Sijmons, R H, Verhoef, S, Kuipers, E J, Morreau, H, Breuning, M H, Tops, C M J, Wijnen, J T, Vasen, H F A, Fodde, R, Hes, F J

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Is surveillance of the small bowel indicated for Lynch syndrome families? von ten Kate, G L, Kleibeuker, J H, Nagengast, F M, Craanen, M, Cats, A, Menko, F H, Vasen, H F A

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Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion von Rijken, J.A., Niemeijer, N.D., Corssmit, E.P.M., Jonker, M.A., Leemans, C.R., Menko, F.H., Hensen, E.F.

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TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes von Ruijs, Marielle W G, Verhoef, Senno, Rookus, Matti A, Pruntel, Roelof, van der Hout, Annemarie H, Hogervorst, Frans B L, Kluijt, I, Sijmons, Rolf H, Aalfs, Cora M, Wagner, Anja, Ausems, Margreet G E M, Hoogerbrugge, Nicoline, van Asperen, Christi J, Gomez Garcia, Encarna B, Meijers-Heijboer, Hanne, ten Kate, Leo P, Menko, Fred H, van 't Veer, Laura J

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Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect von de Vos tot Nederveen Cappel, W H, Buskens, E, van Duijvendijk, P, Cats, A, Menko, F H, Griffioen, G, Slors, J F, Nagengast, F M, Kleibeuker, J H, Vasen, H F A

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Highly variable clinical manifestations in a large family with a novel GATA2 mutation von Mutsaers, P G N J, van de Loosdrecht, A A, Tawana, K, Bödör, C, Fitzgibbon, J, Menko, F H

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis von Vasen, HF, Wijnen, JT, Menko, FH, Kleibeuker, JH, Taal, BG, Griffioen, G, Nagengast, FM, Meijers-Heijboer, EH, Bertario, L, Varesco, L, Bisgaard, ML, Mohr, J, Fodde, R, Khan, PM

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Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach von Gille, J J P, Hogervorst, F B L, Pals, G, Wijnen, J Th, van Schooten, R J, Dommering, C J, Meijer, G A, Craanen, M E, Nederlof, P M, de Jong, D, McElgunn, C J, Schouten, J P, Menko, F H

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Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes von Menko, FH, Kneepkens, CMF, De Leeuw, N, Peeters, EAJ, Van Maldergem, L, Kamsteeg, EJ, Davidson, R, Rozendaal, L, Lasham, CA, Peeters-Scholte, CMP, Jansweijer, MC, Hilhorst-Hofstee, Y, Gille, JJP, Heins, YM, Nieuwint, AWM, Sistermans, EA

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Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations von Johannesma, PC, van der Klift, HM, van Grieken, NCT, Troost, D, te Riele, H, Jacobs, MAJM, Postma, TJ, Heideman, DAM, Tops, CMJ, Wijnen, JT, Menko, FH

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Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer von Piek, Jurgen M. J., van Diest, Paul J., Zweemer, Ronald P., Jansen, Jan W., Poort-Keesom, Ria J. J., Menko, Fred H., Gille, Johan J. P., Jongsma, Ans P. M., Pals, Gerard, Kenemans, Peter, Verheijen, René H. M.

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Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA 1/2-test results von Vos, J, Oosterwijk, JC, Gómez-García, E, Menko, FH, Jansen, AM, Stoel, RD, van Asperen, CJ, Tibben, A, Stiggelbout, AM

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Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data von van der Groep, P, Bouter, A, van der Zanden, R, Siccama, I, Menko, F H, Gille, J J P, van Kalken, C, van der Wall, E, Verheijen, R H M, van Diest, P J

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