Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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High Frequency of CNV Mutations in Combined Schizophrenia and Epilepsy


ABSTRACT: Agilent custom designed array comparative genomic hybridization (CGH) was performed on 235 samples with a dual diagnosis of schizophrenia and epilepsy and 80 samples with a dual diagnosis of bipolar and epilpsy. ArrayCGH on 191 psychiatric screened controls was also performed. A common male reference was used for all samples and controls. Samples and controls were obtained from the NIMH cell line repositories. 235 samples with a dual diagnosis of schizophrenia and epilepsy, 80 samples with a dual diagnosis of bipolar and epilepsy, and 191 psychiatric screened controls

ORGANISM(S): Homo sapiens

SUBMITTER: April Hall 

PROVIDER: E-GEOD-23703 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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