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Showing 1 - 10 results of 10 for search '"Genetic Variation."', query time: 0.02s Refine Results
  1. 1
    Genomic disorders mechanisms for copy number variation (CNV) and clinical implementation of high-resolution genome analysis /

    Genomic disorders mechanisms for copy number variation (CNV) and clinical implementation of high-resolution genome analysis /

    Published 2009
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  2. 2
    Databases for CNV in control and disease populations

    Databases for CNV in control and disease populations

    Published 2009
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  3. 3
    Indels, CNVs and the spectrum of human genome variation

    Indels, CNVs and the spectrum of human genome variation

    Published 2009
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  4. 4
    Population genetics of structural variation

    Population genetics of structural variation

    Published 2009
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  5. 5
    Structural variants and susceptibility to common human disorders

    Structural variants and susceptibility to common human disorders

    Published 2009
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  6. 6
    CNVs in human genomes

    CNVs in human genomes

    Published 2009
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  7. 7
    Array comparative genomic hybridisation to characterise copy number variation in the human genome

    Array comparative genomic hybridisation to characterise copy number variation in the human genome

    Published 2009
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  8. 8
    Quantitative CNV testing in molecular diagnostics

    Quantitative CNV testing in molecular diagnostics

    Published 2009
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  9. 9
    The future of CNVs sequence based resolution and links to human disease, part 1 of 2 /

    The future of CNVs sequence based resolution and links to human disease, part 1 of 2 /

    Published 2017
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    Series (Copy number variation)
    Series (Biomarkers)
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  10. 10
    The future of CNVs sequence based resolution and links to human disease, (part 2 of 2) /

    The future of CNVs sequence based resolution and links to human disease, (part 2 of 2) /

    Published 2017
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    Series (Copy number variation)
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