Your selections:
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome
- Tan, T. Y., Aftimos, S., Slavotinek, A., Hogue, J., Moeschler, J. B., Ozmore, J., Widmer, R., Savarirayan, R., Peters, G., Worgan, L., Susman, R., Wilson, M., Ghedia, S., Kirk, E. P., Love, D., Ronan, A., Darmanian, A.
The adult phenotype in Costello syndrome
- White, S. M., Graham, J. M., Kerr, B., Gripp, K., Weksberg, R., Cytrynbaum, C., Reeder, J. L., Stewart, F. J., Edwards, Matthew, Wilson, M., Bankier, A.
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