Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature

MLA

Makay, Prince, et al. “Greig Cephalopolysyndactyly Contiguous Gene Syndrome in a Congolese Patient Co-Occurring with Sickle Cell Anemia, and Review of Literature.” Clinical Dysmorphology, vol. 34, no. 2, Apr. 2025, pp. 44–48. EBSCOhost, https://doi.org/10.1097/MCD.0000000000000510.

APA

Makay, P., Fasquelle, C., Mubungu, G., Ekolo, E., Mupuala, A., Fuanani, P., Sonet, I., Charloteaux, B., Palmeira, L., Gatot, J.-S., Lukusa Tshilobo, P., Bours, V., Devriendt, K., & Lumaka, A. (2025). Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature. Clinical Dysmorphology, 34(2), 44–48. https://doi.org/10.1097/MCD.0000000000000510

Chicago

Makay, Prince, Corinne Fasquelle, Gerrye Mubungu, Esther Ekolo, Aimée Mupuala, Patrick Fuanani, Ines Sonet, et al. 2025. “Greig Cephalopolysyndactyly Contiguous Gene Syndrome in a Congolese Patient Co-Occurring with Sickle Cell Anemia, and Review of Literature.” Clinical Dysmorphology 34 (2): 44–48. doi:10.1097/MCD.0000000000000510.