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).
doi: 10.1002/ajmg.a.30407
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).
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
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
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