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  1. 1
    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)
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  2. 2
    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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  3. 3
    Copy number variation in mental retardation

    Copy number variation in mental retardation

    Published 2009
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  4. 4
    Copy number variation in neuropsychiatric disorders

    Copy number variation in neuropsychiatric disorders

    Published 2009
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  5. 5
    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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  6. 6
    Mendelian CNV mutations

    Mendelian CNV mutations

    Published 2009
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  7. 7
    Population genetics of structural variation

    Population genetics of structural variation

    Published 2009
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  8. 8
    The case for offering all women amniocentesis and chromosomal microarray analysis

    The case for offering all women amniocentesis and chromosomal microarray analysis

    Published 2009
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  9. 9
    Copy number variation in association studies of human disease

    Copy number variation in association studies of human disease

    Published 2009
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  10. 10
    Quantitative CNV testing in molecular diagnostics

    Quantitative CNV testing in molecular diagnostics

    Published 2009
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  11. 11
    Williams-Beuren syndrome locus a model of CNV affecting gene dosage and phenotypes /

    Williams-Beuren syndrome locus a model of CNV affecting gene dosage and phenotypes /

    Published 2009
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  12. 12
    Databases for CNV in control and disease populations

    Databases for CNV in control and disease populations

    Published 2009
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  13. 13
    Indels, CNVs and the spectrum of human genome variation

    Indels, CNVs and the spectrum of human genome variation

    Published 2009
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  14. 14
    Structural variants and susceptibility to common human disorders

    Structural variants and susceptibility to common human disorders

    Published 2009
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  15. 15
    Copy number variation

    Copy number variation

    Published 2009
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  16. 16
    CNVs in human genomes

    CNVs in human genomes

    Published 2009
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  17. 17
    CNVs and clinical diagnosis

    CNVs and clinical diagnosis

    Published 2009
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  18. 18
    Genome structure and expression

    Genome structure and expression

    Published 2009
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  19. 19
    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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  20. 20
    Mechanisms of human genetic disease

    Mechanisms of human genetic disease

    Published 2021
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