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Emoto Y, Emoto H, Fujle W, Wakakura M (2007). "Uncorrectable Oblique Astigmatism and Impaired Binocular Vision in Case of Orbital Cherubism". Neuro-ophthalmology. 31 (5–6): 191–195. doi:10.1080/01658100701648553. S2CID71602769.
van Capelle CI, Hogeman PH, van der Sijs-Bos CJ, et al. (September 2007). "Neurofibromatosis presenting with a cherubism phenotype". European Journal of Pediatrics. 166 (9): 905–9. doi:10.1007/s00431-006-0334-6. PMID17120035. S2CID1563997.
Peñarrocha, Miguel; Bonet, Jaime; Mínguez, Juan Manuel; Bagán, José Vicente; Vera, Francisco; Mínguez, Ignacio (2006-06-01). "Cherubism: a clinical, radiographic, and histopathologic comparison of 7 cases". Journal of Oral and Maxillofacial Surgery. 64 (6): 924–930. doi:10.1016/j.joms.2006.02.003. ISSN0278-2391. PMID16713807.
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fibrousdysplasia.org
"About Cherubism". FibrousDysplasia.org. Fibrous Dysplasia Foundation. Retrieved 5 November 2017.
van Capelle CI, Hogeman PH, van der Sijs-Bos CJ, et al. (September 2007). "Neurofibromatosis presenting with a cherubism phenotype". European Journal of Pediatrics. 166 (9): 905–9. doi:10.1007/s00431-006-0334-6. PMID17120035. S2CID1563997.
Peñarrocha, Miguel; Bonet, Jaime; Mínguez, Juan Manuel; Bagán, José Vicente; Vera, Francisco; Mínguez, Ignacio (2006-06-01). "Cherubism: a clinical, radiographic, and histopathologic comparison of 7 cases". Journal of Oral and Maxillofacial Surgery. 64 (6): 924–930. doi:10.1016/j.joms.2006.02.003. ISSN0278-2391. PMID16713807.
Jones, W. A.; Gerrie, J.; Pritchard, J. (1950). "Cherubism--familial fibrous dysplasia of the jaws". The Journal of Bone and Joint Surgery. British Volume. 32-B (3): 334–347. doi:10.1302/0301-620X.32B3.334. PMID14778852.
Emoto Y, Emoto H, Fujle W, Wakakura M (2007). "Uncorrectable Oblique Astigmatism and Impaired Binocular Vision in Case of Orbital Cherubism". Neuro-ophthalmology. 31 (5–6): 191–195. doi:10.1080/01658100701648553. S2CID71602769.
van Capelle CI, Hogeman PH, van der Sijs-Bos CJ, et al. (September 2007). "Neurofibromatosis presenting with a cherubism phenotype". European Journal of Pediatrics. 166 (9): 905–9. doi:10.1007/s00431-006-0334-6. PMID17120035. S2CID1563997.