10 results on '"Grinton, Bronwyn E"'
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2. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
3. Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes
4. Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
5. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance
6. Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3
7. SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum
8. Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
9. Invited Comments on the Shostak and Ottman Review: Comment
10. Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families
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