Genomics

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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.

ORGANISM(S): Homo sapiens

PROVIDER: GSE23703 | GEO | 2010/12/31

SECONDARY ACCESSION(S): PRJNA130899

REPOSITORIES: GEO

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