Dobson, S. M., Kiss, C., Borschneck, D., Heath, K. E., Gross, A., Glucksman, M. J., & Guerin, A. (2022). Novel FGF9 variant contributes to multiple synostoses syndrome 3. American journal of medical genetics. Part A, 188(7), 2162-2167. https://doi.org/10.1002/ajmg.a.62729
Citace podle Chicago (17th ed.)Dobson, Stephanie M., Courtney Kiss, Daniel Borschneck, Karen E. Heath, Adrian Gross, Marc J. Glucksman, a Andrea Guerin. "Novel FGF9 Variant Contributes to Multiple Synostoses Syndrome 3." American Journal of Medical Genetics. Part A 188, no. 7 (2022): 2162-2167. https://doi.org/10.1002/ajmg.a.62729.
Citace podle MLA (9th ed.)Dobson, Stephanie M., et al. "Novel FGF9 Variant Contributes to Multiple Synostoses Syndrome 3." American Journal of Medical Genetics. Part A, vol. 188, no. 7, 2022, pp. 2162-2167, https://doi.org/10.1002/ajmg.a.62729.