Pages that link to "Q35152981"
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The following pages link to Genetic testing in epilepsy: what should you be doing? (Q35152981):
Displaying 17 items.
- Seizures and X-linked intellectual disability (Q24594966) (← links)
- Genetic testing in the epilepsies-developments and dilemmas (Q33874944) (← links)
- ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies (Q33888574) (← links)
- Genetic testing preferences in families containing multiple individuals with epilepsy (Q34516966) (← links)
- Epilepsy and autism: is there a special relationship? (Q35840112) (← links)
- Parents' interest in genetic testing of their offspring in multiplex epilepsy families. (Q36552449) (← links)
- Genomic biomarkers of SUDEP in brain and heart (Q37707209) (← links)
- Unexplained Early Infantile Epileptic Encephalopathy in Han Chinese Children: Next-Generation Sequencing and Phenotype Enriching (Q37741362) (← links)
- Genetic testing of epileptic encephalopathies of infancy: an approach. (Q38068314) (← links)
- Precision medicine is here, break out your wallet (Q38283688) (← links)
- Attitudes Toward Epilepsy Genetics Testing Among Adult and Pediatric Epileptologists-Results of a Q-PULSE Survey (Q38350456) (← links)
- SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability (Q39027820) (← links)
- Clinical utility of genetic testing in pediatric drug-resistant epilepsy: a pilot study. (Q39146974) (← links)
- Genotype & Phenotype of Ohtahara Syndrome-What's SCN2A Got to Do With It? A Clinician's Read (Q42935128) (← links)
- Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes (Q48585931) (← links)
- Alphabet Soup: Recurrent De Novo Mutations in Novel Genes Causing Developmental and Epileptic Encephalopathies. (Q52578332) (← links)
- Multimodal Analysis of Missense Variants Improves Interpretation of Clinically Relevant Variants in Dravet Syndrome (Q64106923) (← links)