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1 Ergebnisse
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Copy number variant analysis from exome data in 349 patient..:
Allen, Andrew S
;
Berkovic, Samuel F
;
Coe, Bradley P
...
qt3438h024. , 2015
Link:
https://escholarship.org/uc/item/3438h024
RT Journal T1
Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3438h024&Exemplar=1&LAN=DE A1 Allen, Andrew S A1 Berkovic, Samuel F A1 Coe, Bradley P A1 Cook, Joseph A1 Cossette, Patrick A1 Delanty, Norman A1 Dlugos, Dennis A1 Eichler, Evan E A1 Epstein, Michael P A1 Glauser, Tracy A1 Goldstein, David B A1 Heinzen, Erin L A1 Johnson, Michael R A1 Krumm, Nik A1 Kuzniecky, Ruben A1 Lowenstein, Daniel H A1 Marson, Anthony G A1 Mefford, Heather C A1 Nelson, Ben A1 Esmaeeli Nieh, Sahar A1 O'Brien, Terence J A1 Ottman, Ruth A1 Petrou, Stephen A1 Petrovski, Slavé A1 Poduri, Annapurna A1 Raja, Archana A1 Ruzzo, Elizabeth K A1 Scheffer, Ingrid E A1 Sherr, Elliott A1 Abou‐Khalil, Bassel A1 Alldredge, Brian K A1 Andermann, Eva A1 Andermann, Frederick A1 Amron, Dina A1 Bautista, Jocelyn F A1 Boro, Alex A1 Cascino, Gregory A1 Consalvo, Damian A1 Crumrine, Patricia A1 Devinsky, Orrin A1 Fiol, Miguel A1 Fountain, Nathan B A1 French, Jacqueline A1 Friedman, Daniel A1 Geller, Eric B A1 Glynn, Simon A1 Haut, Sheryl R A1 Hayward, Jean A1 Helmers, Sandra L A1 Joshi, Sucheta A1 Kanner, Andres A1 Kirsch, Heidi E A1 Knowlton, Robert C A1 Kossoff, Eric H A1 Kuperman, Rachel A1 McGuire, Shannon M A1 Motika, Paul V A1 Novotny, Edward J A1 Paolicchi, Juliann M A1 Parent, Jack A1 Park, Kristen A1 Shellhaas, Renée A A1 Shih, Jerry J A1 Singh, Rani A1 Sirven, Joseph A1 Smith, Michael C A1 Sullivan, Joe A1 Thio, Liu Lin A1 Venkat, Anu A1 Vining, Eileen PG A1 Von Allmen, Gretchen K A1 Weisenberg, Judith L A1 Widdess‐Walsh, Peter A1 Winawer, Melodie R PB eScholarship, University of California YR 2015 K1 Biomedical and Clinical Sciences K1 Neurosciences K1 Clinical Sciences K1 Neurodegenerative K1 Genetics K1 Intellectual and Developmental Disabilities (IDD) K1 Epilepsy K1 Pediatric K1 Clinical Research K1 Brain Disorders K1 Human Genome K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adult K1 Child K1 Preschool K1 Cohort Studies K1 DNA Copy Number Variations K1 Exome K1 Female K1 Humans K1 Infant K1 Newborn K1 Lennox Gastaut Syndrome K1 Male K1 Parents K1 Sequence Analysis K1 DNA K1 Spasms K1 Infantile K1 Epilepsy Phenome/Genome Project Epi4K Consortium K1 Neurology & Neurosurgery JF qt3438h024 LK http://dx.doi.org/https://escholarship.org/uc/item/3438h024 DO https://escholarship.org/uc/item/3438h024 SF ELIB - SuUB Bremen
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