Design of the BRISC study: a multicentre controlled clinical trial to optimize the communication of breast cancer risks in genetic counselling

by Menko Fred H, Oosterwijk Jan C, van Asperen Christi J, Henneman Lidewij, Ockhuysen-Vermey Caroline F, Timmermans Daniëlle RM
Published 2008-10-01

Colorectal Cancer in the Family: Psychosocial Distress and Social Issues in the Years Following Genetic Counselling

by Bleiker Eveline MA, Menko Fred H, Kluijt Irma, Taal Babs G, Gerritsma Miranda A, Wever Lidwina DV, Aaronson Neil K
Published 2007-06-01

The contribution of <it>CHEK2 </it>to the <it>TP53</it>-negative Li-Fraumeni phenotype

by Ruijs Marielle WG, Broeks Annegien, Menko Fred H, Ausems Margreet GEM, Wagner Anja, Oldenburg Rogier, Meijers-Heijboer Hanne, van't Veer Laura J, Verhoef Senno
Published 2009-02-01

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

by Wong Nora, Ferrando Barbara, Pasini Barbara, Menko Fred H, Oomen Peter HN, Jansen Jeroen C, Weiss Marjan M, van Minderhout Ivonne, Bayley Jean-Pierre, Alpert Lesley C, Williams Rosie, Blair Edward, Devilee Peter, Taschner Peter EM
Published 2006-01-01

A novel pathogenic <it>MLH1 </it>missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

by van Riel Els, Ausems Margreet GEM, Hogervorst Frans BL, Kluijt Irma, van Gijn Marielle E, van Echtelt Jeanne, Scheidel-Jacobse Karen, Hennekam Eric FAM, Stulp Rein P, Vos Yvonne J, Offerhaus G Johan A, Menko Fred H, Gille Johan JP
Published 2010-08-01