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Diagnostic implications of genetic copy number variation in..:

Coppola, A ; Cellini, E ; Stamberger, H...
https://discovery.ucl.ac.uk/id/eprint/10071080/1/Coppola_et_al-2019-Epilepsia.pdf. , 2019

Link: https://discovery.ucl.ac.uk/id/eprint/10071080/1/Coppo..

RT Journal
T1 <Title>Diagnostic implications of genetic copy number variation in epilepsy plus</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10071080&Exemplar=1&LAN=DE
				
A1 Coppola, A
A1 Cellini, E
A1 Stamberger, H
A1 Saarentaus, E
A1 Cetica, V
A1 Lal, D
A1 Djémié, T
A1 Bartnik-Glaska, M
A1 Ceulemans, B
A1 Helen Cross, J
A1 Deconinck, T
A1 Masi, SD
A1 Dorn, T
A1 Guerrini, R
A1 Hoffman-Zacharska, D
A1 Kooy, F
A1 Lagae, L
A1 Lench, N
A1 Lemke, JR
A1 Lucenteforte, E
A1 Madia, F
A1 Mefford, HC
A1 Morrogh, D
A1 Nuernberg, P
A1 Palotie, A
A1 Schoonjans, A-S
A1 Striano, P
A1 Szczepanik, E
A1 Tostevin, A
A1 Vermeesch, JR
A1 Esch, HV
A1 Paesschen, WV
A1 Waters, JJ
A1 Weckhuysen, S
A1 Zara, F
A1 Jonghe, PD
A1 Sisodiya, SM
A1 Marini, C
A1 EuroEPINOMICS-RES Consortium
A1 EpiCNV Consortium
YR 2019
K1 SNP array
K1 array CGH
K1 copy number variants
K1 epilepsy genes
JF https://discovery.ucl.ac.uk/id/eprint/10071080/1/Coppola_et_al-2019-Epilepsia.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10071080/1/Coppola_et_al-2019-Epilepsia.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10071080/1/Coppola_et_al-2019-Epilepsia.pdf
SF ELIB - SuUB Bremen

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