Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan… - Epilepsia …, 2019 - Wiley Online Library
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan… - Epilepsia …, 2019 - search.proquest.com
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

[PDF][PDF] Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan, J Millichap… - 2019 - researchgate.net
Objective: Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan… - Epilepsia …, 2019 - scholars.northwestern.edu
Objective: Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan, J Millichap… - Epilepsia Open, 2019 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: sec>< jats: title> Objective</jats: title>< jats: p>
Molecular genetic etiologies in epilepsy have become better understood in recent years …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan… - Epilepsia …, 2019 - pubmed.ncbi.nlm.nih.gov
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

[HTML][HTML] Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort …

R Truty, N Patil, R Sankar, J Sullivan, J Millichap… - Epilepsia …, 2019 - ncbi.nlm.nih.gov
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan, J Millichap… - Epilepsia …, 2019 - europepmc.org
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with …

R Truty, N Patil, R Sankar, J Sullivan, J Millichap… - Epilepsia …, 2019 - europepmc.org
Objective Molecular genetic etiologies in epilepsy have become better understood in recent
years, creating important opportunities for precision medicine. Building on these advances …