Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.

MLA

Pansuriya, Twinkal C., et al. “Somatic Mosaic IDH1 and IDH2 Mutations Are Associated with Enchondroma and Spindle Cell Hemangioma in Ollier Disease and Maffucci Syndrome.” Nature Genetics, vol. 43, no. 12, Nov. 2011, pp. 1256–61. EBSCOhost, https://doi.org/10.1038/ng.1004.

APA

Pansuriya, T. C., van Eijk, R., d’Adamo, P., van Ruler, M. A. J. H., Kuijjer, M. L., Oosting, J., Cleton-Jansen, A.-M., van Oosterwijk, J. G., Verbeke, S. L. J., Meijer, D., van Wezel, T., Nord, K. H., Sangiorgi, L., Toker, B., Liegl-Atzwanger, B., San-Julian, M., Sciot, R., Limaye, N., Kindblom, L.-G., … Bovée, J. V. M. G. (2011). Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nature Genetics, 43(12), 1256–1261. https://doi.org/10.1038/ng.1004

Chicago

Pansuriya, Twinkal C, Ronald van Eijk, Pio d’Adamo, Maayke A J H van Ruler, Marieke L Kuijjer, Jan Oosting, Anne-Marie Cleton-Jansen, et al. 2011. “Somatic Mosaic IDH1 and IDH2 Mutations Are Associated with Enchondroma and Spindle Cell Hemangioma in Ollier Disease and Maffucci Syndrome.” Nature Genetics 43 (12): 1256–61. doi:10.1038/ng.1004.