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• W2074668801 endingPage "287" @default.
• W2074668801 startingPage "271" @default.
• W2074668801 abstract "Our understanding of the causes of mental retardation is benefiting greatly from whole-genome scans to detect submicroscopic pathogenic copy number variants (CNVs) that are undetectable by conventional cytogenetic analysis. The current method of choice for performing whole-genome scans for CNVs is array genomic hybridization (AGH). Several platforms are available for AGH, each with its own strengths and limitations. This review discusses considerations that are relevant to the clinical use of whole-genome AGH platforms for the diagnosis of pathogenic CNVs in children with mental retardation. Whole-genome AGH studies are a maturing technology, but their high diagnostic utility assures their increasing use in clinical genetics." @default.
• W2074668801 created "2016-06-24" @default.
• W2074668801 creator A5032669027 @default.
• W2074668801 creator A5051852805 @default.
• W2074668801 date "2007-08-28" @default.
• W2074668801 modified "2023-10-18" @default.
• W2074668801 title "The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility" @default.
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