APA (7th ed.) Citation

Menko, F. H., ter Stege, J. A., van der Kolk, L. E., Jeanson, K. N., Schats, W., Moha, D. A., & Bleiker, E. M. A. (2019). The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: A systematic review of the literature and implications for clinical practice. Familial cancer, 18(1), 127-135. https://doi.org/10.1007/s10689-018-0089-z

Chicago Style (17th ed.) Citation

Menko, Fred H., Jacqueline A. ter Stege, Lizet E. van der Kolk, Kiki N. Jeanson, Winnie Schats, Daoud Ait Moha, and Eveline M A. Bleiker. "The Uptake of Presymptomatic Genetic Testing in Hereditary Breast-ovarian Cancer and Lynch Syndrome: A Systematic Review of the Literature and Implications for Clinical Practice." Familial Cancer 18, no. 1 (2019): 127-135. https://doi.org/10.1007/s10689-018-0089-z.

MLA (9th ed.) Citation

Menko, Fred H., et al. "The Uptake of Presymptomatic Genetic Testing in Hereditary Breast-ovarian Cancer and Lynch Syndrome: A Systematic Review of the Literature and Implications for Clinical Practice." Familial Cancer, vol. 18, no. 1, 2019, pp. 127-135, https://doi.org/10.1007/s10689-018-0089-z.