TY  - GEN
AU  - Striano,Pasquale
AU  - Coppola,Antonietta
AU  - Paravidino,Roberta
AU  - Malacarne,Michela
AU  - Gimelli,Stefania
AU  - Robbiano,Angela
AU  - Traverso,Monica
AU  - Pezzella,Marianna
AU  - Belcastro,Vincenzo
AU  - Bianchi,Amedeo
AU  - Elia,Maurizio
AU  - Falace,Antonio
AU  - Gazzerro,Elisabetta
AU  - Ferlazzo,Edoardo
AU  - Freri,Elena
AU  - Galasso,Roberta
AU  - Gobbi,Giuseppe
AU  - Molinatto,Cristina
AU  - Cavani,Simona
AU  - Zuffardi,Orsetta
AU  - Striano,Salvatore
AU  - Ferrero,Giovanni Battista
AU  - Silengo,Margherita
AU  - Cavaliere,Maria Luigia
AU  - Benelli,Matteo
AU  - Magi,Alberto
AU  - Piccione,Maria
AU  - Dagna Bricarelli,Franca
AU  - Coviello,Domenico A
AU  - Fichera,Marco
AU  - Minetti,Carlo
AU  - Zara,Federico
TI  - Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization
SN  - 1538-3687
PY  - 2012///0501
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Computational Biology
KW  - Diagnostic and Statistical Manual of Mental Disorders
KW  - Epilepsy
KW  - genetics
KW  - Female
KW  - Gene Deletion
KW  - Gene Dosage
KW  - Gene Duplication
KW  - Gene Rearrangement
KW  - Genome-Wide Association Study
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - epidemiology
KW  - Italy
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Microarray Analysis
KW  - Middle Aged
KW  - Nervous System Diseases
KW  - Nucleic Acid Hybridization
KW  - Polymerase Chain Reaction
KW  - Prospective Studies
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1001/archneurol.2011.1999
ER  -