The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

Author(s):: Teixeira, N.; Hout, A. van der; Oosterwijk, J.C.; Vos, J.R.; Devilee, P. (0000-0002-8023-2009); Engelen, K. van; Meijers-Heijboer, H.; Luijt, R.B. van der; Kriege, M.; Mensenkamp, A.R.; Rookus, M.A.; Roozendaal, K.E. van; Mourits, M.J.E.; Bock, G.H. de; HEBON

Published: 2018
Publication type: Article / Letter to editor

Date issued: 2018-06-30
Language: English
Is part of: European Journal of Human Genetics (2018), Vol. 26, no. 6, p. 848-857
hdl: 1887/79412
doi: 10.1038/s41431-018-0111-9
URL: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974362/