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Diagnostic implications of genetic copy number variation in..:

Coppola, Antonietta ; Cellini, Elena ; Stamberger, Hannah...
Coppola , A , Cellini , E , Stamberger , H , Saarentaus , E , Cetica , V , Lal , D , Djemie , T , Bartnik-Glaska , M , Ceulemans , B , Cross , J H , Deconinck , T , De Masi , S , Dorn , T , Guerrini , R , Hoffman-Zacharska , D , Kooy , F , Lagae , L , Lench , N , Lemke , J R , Lucenteforte , E , Madia , F , Mefford , H C , Morrogh , D , Nuernberg , P , Palotie , A , Schoonjans , A-S , Striano , P , Szczepanik , E , Tostevin , A , Vermeesch , J R , Van Esch , H , Van Paesschen , W , Waters , J J , Weckhuysen , S , Zara , F , Jonghe , P D , Sisodiya , S M , Marini , C , EuroEPINOMICS RES Consortium , Moller , R S & Hjalgrim , H 2019 , ' Diagnostic implications of genetic copy number variation in epilepsy plus ' , Epilepsia , vol. 60 , no. 4 , pp. 689-706 . https://doi.org/10.1111/epi.14683. , 2019

Link: https://portal.findresearcher.sdu.dk/da/publications/7..

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

UL https://suche.suub.uni-bremen.de/peid=base-ftsydanskunivpub:oai:sdu.dk:publications_7119ad8d-6243-4598-b8c4-a3b7977a8fd9&Exemplar=1&LAN=DE
				
A1 Coppola, Antonietta
A1 Cellini, Elena
A1 Stamberger, Hannah
A1 Saarentaus, Elmo
A1 Cetica, Valentina
A1 Lal, Dennis
A1 Djemie, Tania
A1 Bartnik-Glaska, Magdalena
A1 Ceulemans, Berten
A1 Cross, J. Helen
A1 Deconinck, Tine
A1 De Masi, Salvatore
A1 Dorn, Thomas
A1 Guerrini, Renzo
A1 Hoffman-Zacharska, Dorotha
A1 Kooy, Frank
A1 Lagae, Lieven
A1 Lench, Nicholas
A1 Lemke, Johannes R
A1 Lucenteforte, Ersilia
A1 Madia, Francesca
A1 Mefford, Heather C
A1 Morrogh, Deborah
A1 Nuernberg, Peter
A1 Palotie, Aarno
A1 Schoonjans, An-Sofie
A1 Striano, Pasquale
A1 Szczepanik, Elzbieta
A1 Tostevin, Anna
A1 Vermeesch, Joris R
A1 Van Esch, Hilde
A1 Van Paesschen, Wim
A1 Waters, Jonathan J
A1 Weckhuysen, Sarah
A1 Zara, Federico
A1 Jonghe, Peter De
A1 Sisodiya, Sanjay M
A1 Marini, Carla
A1 Moller, Rikke S
A1 Hjalgrim, Helle
YR 2019
K1 SNP array
K1 array CGH
K1 copy number variants
K1 epilepsy genes
K1 Genetic Predisposition to Disease
K1 Phenotype
K1 Comorbidity
K1 Humans
K1 Epilepsy/complications
K1 Genotype
K1 DNA Copy Number Variations
JF Coppola , A , Cellini , E , Stamberger , H , Saarentaus , E , Cetica , V , Lal , D , Djemie , T , Bartnik-Glaska , M , Ceulemans , B , Cross , J H , Deconinck , T , De Masi , S , Dorn , T , Guerrini , R , Hoffman-Zacharska , D , Kooy , F , Lagae , L , Lench , N , Lemke , J R , Lucenteforte , E , Madia , F , Mefford , H C , Morrogh , D , Nuernberg , P , Palotie , A , Schoonjans , A-S , Striano , P , Szczepanik , E , Tostevin , A , Vermeesch , J R , Van Esch , H , Van Paesschen , W , Waters , J J , Weckhuysen , S , Zara , F , Jonghe , P D , Sisodiya , S M , Marini , C , EuroEPINOMICS RES Consortium , Moller , R S & Hjalgrim , H 2019 , ' Diagnostic implications of genetic copy number variation in epilepsy plus ' , Epilepsia , vol. 60 , no. 4 , pp. 689-706 . https://doi.org/10.1111/epi.14683
LK http://dx.doi.org/https://portal.findresearcher.sdu.dk/da/publications/7119ad8d-6243-4598-b8c4-a3b7977a8fd9
DO https://portal.findresearcher.sdu.dk/da/publications/7119ad8d-6243-4598-b8c4-a3b7977a8fd9
SF ELIB - SuUB Bremen

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