J, K., K, Z., R, G., M, W., J, T., B, S., . . . M, Z. (2019). Sensitive detection of FGFR1 N546K mosaic mutation in patient with encephalocraniocutaneous lipomatosis and pilocytic astrocytoma. American journal of medical genetics. Part A, 179(8), 1622. https://doi.org/10.1002/ajmg.a.61256
Chicago Style (17th ed.) CitationJ, Kordacka, Zakrzewski K, Gruszka R, Witusik-Perkowska M, Taha J, Sikorska B, Liberski PP, and Zakrzewska M. "Sensitive Detection of FGFR1 N546K Mosaic Mutation in Patient with Encephalocraniocutaneous Lipomatosis and Pilocytic Astrocytoma." American Journal of Medical Genetics. Part A 179, no. 8 (2019): 1622. https://doi.org/10.1002/ajmg.a.61256.
MLA (9th ed.) CitationJ, Kordacka, et al. "Sensitive Detection of FGFR1 N546K Mosaic Mutation in Patient with Encephalocraniocutaneous Lipomatosis and Pilocytic Astrocytoma." American Journal of Medical Genetics. Part A, vol. 179, no. 8, 2019, p. 1622, https://doi.org/10.1002/ajmg.a.61256.