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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.

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation

- Jensen, L. R., Amende, M., Gurok, U., Moser, B., Gimmel, V., Tzschach, A., Janecke, A. R., Tariverdian, G., Chelly, J., Fryns, J. P., Van Esch, H., Kleefstra, T., Hamel, B., Moraine, C., Gecz, J., Turner, Gillian, Reinhardt, R., Kalscheuer, V. M., Ropers, H. H., Lenzner, S.

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