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
Chicago Style (17th ed.) CitationDobson, Stephanie M., Courtney Kiss, Daniel Borschneck, Karen E. Heath, Adrian Gross, Marc J. Glucksman, and 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.
MLA (9th ed.) CitationDobson, 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.