Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research

Ron Hochstenbach,Jacobine E. Buizer-Voskamp,J.A.S. Vorstman,Roel A. Ophoff

Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research

2011

Ron Hochstenbach
Jacobine E. Buizer-Voskamp
J.A.S. Vorstman
Roel A. Ophoff

We review the contributions and limitations of genome-wide array-based identification of copy number variants (CNVs) in the clinical diagnostic evaluation of patients with mental retardation (MR) and

Keywords:

SNP array
Biology
Autism
Idiopathic generalized epilepsy
Workflow
Genome
Schizophrenia
Copy-number variation
Bioinformatics
Tourette syndrome
Genome-wide association study
Major depressive disorder

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