F. Menko

Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis

L. Hoefsloot, S. Shanley, M. Breuning, 2011, Clinical genetics.

Genetic defects underlying Peutz–Jeghers syndrome (PJS) and exclusion of the polarity‐associated MARK/Par1 gene family as potential PJS candidates

G. Offerhaus, F. Giardiello, M. Polak, 2007, Clinical genetics.

Childhood brain tumours due to germline bi‐allelic mismatch repair gene mutations

D. Troost, T. Postma, H. te Riele, 2011, Clinical genetics.

Perceiving cancer‐risks and heredity‐likelihood in genetic‐counseling: how counselees recall and interpret BRCA 1/2‐test results

A. Stiggelbout, C. Asperen, J. Oosterwijk, 2011, Clinical genetics.

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

D. Jong, J. Schouten, C. Mcelgunn, 2002, British Journal of Cancer.

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

E. Bongers, P. Postmus, R. Oldenburg, 2011, British Journal of Cancer.