Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I.

MLA

Toledano, Helen, et al. “Homozygosity of MSH2 c.1906G-->C Germline Mutation Is Associated with Childhood Colon Cancer, Astrocytoma and Signs of Neurofibromatosis Type I.” Familial Cancer, vol. 8, no. 3, 2009, pp. 187–94. EBSCOhost, https://doi.org/10.1007/s10689-008-9227-3.

APA

Toledano, H., Goldberg, Y., Kedar-Barnes, I., Baris, H., Porat, R. M., Shochat, C., Bercovich, D., Pikarsky, E., Lerer, I., Yaniv, I., Abeliovich, D., & Peretz, T. (2009). Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I. Familial Cancer, 8(3), 187–194. https://doi.org/10.1007/s10689-008-9227-3

Chicago

Toledano, Helen, Yael Goldberg, Inbal Kedar-Barnes, Hagit Baris, Rinnat M Porat, Chen Shochat, Dani Bercovich, et al. 2009. “Homozygosity of MSH2 c.1906G-->C Germline Mutation Is Associated with Childhood Colon Cancer, Astrocytoma and Signs of Neurofibromatosis Type I.” Familial Cancer 8 (3): 187–94. doi:10.1007/s10689-008-9227-3.