Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations
- Creator: Dibbens, L. M. , Kneen, R. , Ronan, A. , Scheffer, I. E. , Bayly, M. A. , Heron, S. E. , Arsov, T. , Damiano, J. A. , Desai, T. , Gibbs, J. , McKenzie, F. , Mulley, J. C.
- Resource Type: journal article
- Date: 2011
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome
- Creator: 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.
- Resource Type: journal article
- Date: 2009