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doi: 10.1038/sj.ejhg.5201758
So, J., V. Suckow, Z. Kijas, V. Kalscheuer, B. Moser, J. Winter, M. Baars, H. Firth, P. Lunt, B. Hamel, P. Meinecke, C. Moraine, S. Odent, A. Schinzel, J. J. van der Smagt, K. Devriendt, B. Albrecht, G. Gillessen-Kaesbach, I. van der Burgt, F. Petrij, L. Faivre, J. McGaughran, F. McKenzie, J. M. Opitz, T. Cox and S. Schweiger: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. In: American Journal of Medical Genetics Part A 132A, 1, 1-7 (2006).
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So, J., V. Suckow, Z. Kijas, V. M. Kalscheuer, B. Moser, J. Winter, M. Baars, H. Firth, P. Lunt, B. Hamel, P. Meinecke, C. Moraine, S. Odent, A. Schinzel, J. J. van der Smagt, K. Devriendt, B. Albrecht, G. Gillessen-Kaesbach, I. van der Burgt, F. Petrij, L. Faivre, J. McGaughran, F. McKenzie, J. M. Opitz, T. Cox and S. Schweiger: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. In: American Journal of Medical Genetics : Part A 132, 1, 1-7 (2005).
doi: 10.1002/ajmg.a.30407
So, J., V. Suckow, Z. Kijas, V. M. Kalscheuer, B. Moser, J. Winter, M. Baars, H. Firth, P. Lunt, B. Hamel, P. Meinecke, C. Moraine, S. Odent, A. Schinzel, J. J. van der Smagt, K. Devriendt, B. Albrecht, G. Gillessen-Kaesbach, I. van der Burgt, F. Petrij, L. Faivre, J. McGaughran, F. McKenzie, J. M. Opitz, T. Cox and S. Schweiger: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. In: American Journal of Medical Genetics : Part A 132, 1, 1-7 (2005).
doi: 10.1002/ajmg.a.30407
Jensen, L. R., M. Amende, U. Gurok, B. Moser, V. Gimme, A. Tzschach, A. R. Janecke, G. Tariverdian, J. Chelly, J.-P. Fryns, H. Van Esch, T. Kleefstra, B. Hame, C. Moraine, J. Gécz, G. Turner, R. Reinhardt, V. M. Kalscheuer, H.-H. Ropers and S. Lenzner: : Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation. In: American Journal of Human Genetics 76, 2, 227-236 (2005).
doi: 0002-9297/2005/7602-0010
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