Wallace Robyn | Department Of Cytogenetics And Molecular Genetics Centre For Medical Genetics Women's And Child
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Department Of Cytogenetics And Molecular Genetics Centre For Medical Genetics Women's And Child | 論文
- Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)
- Is Variation in the GABA(B) Receptor 1 Gene Associated with Temporal Lobe Epilepsy?
- The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
- Febrile Convulsions and Genetic Susceptibility : Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit