[HTML][HTML] Commentary: 2016 Clinical Epilepsia Prize
DT Miller - Epilepsia, 2016 - ncbi.nlm.nih.gov
The Clinical Epilepsia Prize for 2016 is being awarded to Mercimek-Mahmutoglu et al. for
their paper “Diagnostic yield of genetic testing in epileptic encephalopathy in childhood,” …
their paper “Diagnostic yield of genetic testing in epileptic encephalopathy in childhood,” …
[引用][C] Commentary: 2016 Clinical Epilepsia Prize
DT Miller - Epilepsia, 2016 - infona.pl
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[引用][C] Commentary: 2016 Clinical Epilepsia Prize
DT Miller - Epilepsia, 2016 - Wiley Online Library
most common type of sequence change identified (53%), and there is often difficulty in
determining the clinical significance of missense mutations. Parental testing helped …
determining the clinical significance of missense mutations. Parental testing helped …
[引用][C] Commentary: 2016 Clinical Epilepsia Prize
DT Miller - Epilepsia, 2016 - pubmed.ncbi.nlm.nih.gov
Commentary: 2016 Clinical Epilepsia Prize.
DT Miller - Epilepsia (Series 4), 2016 - search.ebscohost.com
Commentary: 2016 Clinical Epilepsia Prize Page 1 Dr. David T. Miller is a medical geneticist
specializing in genetic testing for neurodevelopmental disorders. The Clinical Epilepsia Prize …
specializing in genetic testing for neurodevelopmental disorders. The Clinical Epilepsia Prize …
Commentary: 2016 Clinical Epilepsia Prize.
DT Miller - Epilepsia, 2016 - europepmc.org
The Clinical Epilepsia Prize for 2016 is being awarded to Mercimek-Mahmutoglu et al. for
their paper “Diagnostic yield of genetic testing in epileptic encephalopathy in childhood,” …
their paper “Diagnostic yield of genetic testing in epileptic encephalopathy in childhood,” …