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Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations

- So, J., Suckow, V., Kijas, Z., Kalscheuer, V., Moser, B., Winter, J., Baars, M., Firth, H., Lunt, P., Hamel, B., Meinecke, P., Moraine, C., Odent, S., Schinzel, A., van der Smagt, J. J., Devriendt, K., Albrecht, B., Gillessen-Kaesbach, G., van der Burgt, I., Petrij, F., Faivre, L., McGaughran, J., McKenzie, Fiona, Opitz, J. M., Cox, T., Schweiger, S.

Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS)

- Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., Thierry, P., Edwards, Matthew, Konig, R., Rusu, C., Schweiger, S., Thompson, E., Tinschert, S., Stewart, F., Wieacker, P.

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