Novel UBE3Bmutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population

MLA

Albakheet, AlBandary, et al. “Novel UBE3Bmutations: Report of Eight Patients with Kaufman Oculocerebrofacial Syndrome with Additional Clinical Findings from a Highly Consanguineous Population.” Clinical Dysmorphology, vol. 33, no. 2, Apr. 2024, pp. 55–62. EBSCOhost, https://doi.org/10.1097/MCD.0000000000000486.

APA

Albakheet, A., Almuallami, D., Almass, R., Qari, A., Kenana, R., AlQudairy, H., Huma, R., Binomar, H., Wakil, S. M., Alowain, M., Colak, D., Kaya, N., & AlSayed, M. D. (2024). Novel UBE3Bmutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population. Clinical Dysmorphology, 33(2), 55–62. https://doi.org/10.1097/MCD.0000000000000486

Chicago

Albakheet, AlBandary, Duaa Almuallami, Rawan Almass, Alya Qari, Rosan Kenana, Hanan AlQudairy, Rozeena Huma, et al. 2024. “Novel UBE3Bmutations: Report of Eight Patients with Kaufman Oculocerebrofacial Syndrome with Additional Clinical Findings from a Highly Consanguineous Population.” Clinical Dysmorphology 33 (2): 55–62. doi:10.1097/MCD.0000000000000486.