Williams syndrome and chromosome 18.

Por Menko, F H, Stouthart, P J
Publicado em 1992

Is surveillance of the small bowel indicated for Lynch syndrome families?

Por Kate, G L ten, Kleibeuker, J H, Nagengast, F M, Craanen, M, Cats, A, Menko, F H, Vasen, H F A
Publicado em 2007

Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds

Por Scheenstra, R, Rijcken, F E M, Koornstra, J J, Hollema, H, Fodde, R, Menko, F H, Sijmons, R H, Bijleveld, C M A, Kleibeuker, J H
Publicado em 2003

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.

Por Pollak, M R, Chou, Y H, Marx, S J, Steinmann, B, Cole, D E, Brandi, M L, Papapoulos, S E, Menko, F H, Hendy, G N, Brown, E M
Publicado em 1994

Clinical heterogeneity of familial colorectal cancer and its influence on screening protocols.

Por Vasen, H F, Taal, B G, Griffioen, G, Nagengast, F M, Cats, A, Menko, F H, Oskam, W, Kleibeuker, J H, Offerhaus, G J, Khan, P M
Publicado em 1994

Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome

Por Johannesma, P. C., van Moorselaar, R. J. A., Horenblas, S., van der Kolk, L. E., Thunnissen, E., van Waesberghe, J. H. T. M., Menko, F. H., Postmus, P. E.
Publicado em 2014

Accumulation of p53 protein is frequent in ovarian cancers associated with BRCA1 and BRCA2 germline mutations.

Por Zweemer, R P, Shaw, P A, Verheijen, R M, Ryan, A, Berchuck, A, Ponder, B A, Risch, H, McLaughlin, J R, Narod, S A, Menko, F H, Kenemans, P, Jacobs, I J
Publicado em 1999

Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

Por 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
Publicado em 2003

Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data

Por 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
Publicado em 2006

STRAD in Peutz-Jeghers syndrome and sporadic cancers

Por de Leng, W W J, Keller, J J, Luiten, S, Musler, A R, Jansen, M, Baas, A F, de Rooij, F W M, Gille, J J P, Menko, F H, Offerhaus, G J A, Weterman, M A J
Publicado em 2005

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

Por Gille, J J P, Hogervorst, F B L, Pals, G, Wijnen, JTh, 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
Publicado em 2002

Risk of spontaneous pneumothorax due to air travel and diving in patients with Birt–Hogg–Dubé syndrome

Por Johannesma, P. C., van de Beek, I., van der Wel, J. W. T., Paul, M. A., Houweling, A. C., Jonker, M. A., van Waesberghe, J. H. T. M., Reinhard, R., Starink, Th. M., van Moorselaar, R. J. A., Menko, F. H., Postmus, P. E.
Publicado no Springerplus (2016)

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

Por Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Publicado no Fam Cancer (2016)

Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2

Por Ligtenberg, M J L, Hogervorst, F B L, Willems, H W, Arts, P J W, Brink, G, Hageman, S, Bosgoed, E A J, Looij, E Van der, Rookus, M A, Devilee, P, Vos, E M A W, Wigbout, G, Struycken, P M, Menko, F H, Rutgers, E J Th, Hoefsloot, E H, Mariman, E C M, Brunner, H G, Veer, L J Van't
Publicado em 1999

STK11 status and intussusception risk in Peutz‐Jeghers syndrome

Por Hearle, N, Schumacher, V, Menko, F H, Olschwang, S, Boardman, L A, Gille, J J P, Keller, J J, Westerman, A M, Scott, R J, Lim, W, Trimbath, J D, Giardiello, F M, Gruber, S B, Offerhaus, G J A, Rooij, F W M D E, Wilson, J H P, Hansmann, A, Möslein, G, Royer‐Pokora, B, Vogel, T, Phillips, R K S, Spigelman, A D, Houlston, R S
Publicado em 2006

Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

Por 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
Publicado em 2011

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

Por Peelen, T., van Vliet, M., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., van der Luijt, R., van der Hout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., van Leeuwen, I., Newman, B., Plandsoen, M., van der Est, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., van Asperen, C. J., Meijers-Heijboer, H., Klijn, J. G. M., de Greve, J., King, M.-C., Menko, F. H., Brunner, H. G., Halley, D., van Ommen, G.-J. B., Vasen, H. F. A., Cornelisse, C. J., van 'tVeer, L. J., de Knijff, P., Bakker, E., Devilee, P.
Publicado em 1997