CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
- Voineagu, I., Huang, L., Field, M., Gecz, J., Geschwind, D., Winden, K., Lazaro, M., Haan, E., Nelson, J., McGaughran, J., Nguyen, L. S., Friend, K., Hackett, A.
- Creator: Voineagu, I. , Huang, L. , Field, M. , Gecz, J. , Geschwind, D. , Winden, K. , Lazaro, M. , Haan, E. , Nelson, J. , McGaughran, J. , Nguyen, L. S. , Friend, K. , Hackett, A.
- Resource Type: journal article
- Date: 2012
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.
- 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
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