Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.

MLA

Lynch, Henry T., et al. “Phenotypic and Genotypic Heterogeneity of Lynch Syndrome: A Complex Diagnostic Challenge.” Familial Cancer, vol. 17, no. 3, July 2018, pp. 403–14. EBSCOhost, https://doi.org/10.1007/s10689-017-0053-3.

APA

Lynch, H. T., Lanspa, S., Shaw, T., Casey, M. J., Rendell, M., Stacey, M., Townley, T., Snyder, C., Hitchins, M., & Bailey-Wilson, J. (2018). Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge. Familial Cancer, 17(3), 403–414. https://doi.org/10.1007/s10689-017-0053-3

Chicago

Lynch, Henry T, Stephen Lanspa, Trudy Shaw, Murray Joseph Casey, Marc Rendell, Mark Stacey, Theresa Townley, Carrie Snyder, Megan Hitchins, and Joan Bailey-Wilson. 2018. “Phenotypic and Genotypic Heterogeneity of Lynch Syndrome: A Complex Diagnostic Challenge.” Familial Cancer 17 (3): 403–14. doi:10.1007/s10689-017-0053-3.