Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations
- Creator: 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.
- Resource Type: journal article
- Date: 2005
Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation
- Creator: 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.
- Resource Type: journal article
- Date: 2005