Cite
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
MLA
Peluso, Francesca, et al. “Deep Phenotyping of the Neuroimaging and Skeletal Features in KBG Syndrome: A Study of 53 Patients and Review of the Literature.” Journal of Medical Genetics, vol. 60, no. 12, Nov. 2023, pp. 1224–34. EBSCOhost, https://doi.org/10.1136/jmg-2023-109141.
APA
Peluso, F., Caraffi, S. G., Contrò, G., Valeri, L., Napoli, M., Carboni, G., Seth, A., Zuntini, R., Coccia, E., Astrea, G., Bisgaard, A.-M., Ivanovski, I., Maitz, S., Brischoux-Boucher, E., Carter, M. T., Dentici, M. L., Devriendt, K., Bellini, M., Digilio, M. C., … Bayat, A. (2023). Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature. Journal of Medical Genetics, 60(12), 1224–1234. https://doi.org/10.1136/jmg-2023-109141
Chicago
Peluso, Francesca, Stefano G Caraffi, Gianluca Contrò, Lara Valeri, Manuela Napoli, Giorgia Carboni, Alka Seth, et al. 2023. “Deep Phenotyping of the Neuroimaging and Skeletal Features in KBG Syndrome: A Study of 53 Patients and Review of the Literature.” Journal of Medical Genetics 60 (12): 1224–34. doi:10.1136/jmg-2023-109141.