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Diagnostic implications of genetic copy number variation in..:
EuroEPINOMICS-RES Consortium
;
EpiCNV Consortium
;
Coppola, Antonietta
...
10.1111/epi.14683. , 2019
Link:
http://hdl.handle.net/10138/301411
RT Journal T1 <Title>Diagnostic implications of genetic copy number variation in epilepsy plus</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_301411&Exemplar=1&LAN=DE A1 EuroEPINOMICS-RES Consortium A1 EpiCNV Consortium A1 Coppola, Antonietta A1 Cellini, Elena A1 Saarentaus, Elmo A1 Palotie, Aarno A1 Lehesjioki, Anna-Elina A1 von Spiczak, Sarah PB Wiley YR 2019 K1 array CGH K1 copy number variants K1 epilepsy genes K1 SNP array K1 DE-NOVO MUTATIONS K1 MOLECULAR CHARACTERIZATION K1 CHROMOSOMAL MICROARRAY K1 ILAE COMMISSION K1 ONSET EPILEPSY K1 RORB GENE K1 PATIENT K1 ENCEPHALOPATHY K1 DISABILITIES K1 PHENOTYPE K1 Neurosciences K1 Neurology and psychiatry K1 Genetics K1 developmental biology K1 physiology JF 10.1111/epi.14683 LK http://hdl.handle.net/10138/301411 DO http://hdl.handle.net/10138/301411 SF ELIB - SuUB Bremen
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