Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations von Foster, B.L., Ramnitz, M.S., Gafni, R.I., Burke, A.B., Boyce, A.M., Lee, J.S., Wright, J.T., Akintoye, S.O., Somerman, M.J., Collins, M.T.

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Hypercementosis Associated with ENPP1 Mutations and GACI von Thumbigere-Math, V., Alqadi, A., Chalmers, N.I., Chavez, M.B., Chu, E.Y., Collins, M.T., Ferreira, C.R., FitzGerald, K., Gafni, R.I., Gahl, W.A., Hsu, K.S., Ramnitz, M.S., Somerman, M.J., Ziegler, S.G., Foster, B.L.

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Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature von Chakhtoura, M., Ramnitz, M.S., Khoury, N., Nemer, G., Shabb, N., Abchee, A., Berberi, A., Hourani, M., Collins, M., Ichikawa, S., El Hajj Fuleihan, G.

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