Özdemir, Ö. M. A., Tancer-Elçi, H., Polat, A., Güçtürk, İ., Tepeli, E., Zeybek, S., & Ayaz, A. (2016). Familial mutation in Caffey disease with reduced penetrance: A case report. The Turkish Journal of Pediatrics, 58(6), 650-653. https://doi.org/10.24953/turkjped.2016.06.011