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  1. 1
    CNVs and clinical diagnosis

    CNVs and clinical diagnosis

    Published 2009
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  2. 2
    Copy number variation

    Copy number variation

    Published 2009
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  3. 3
    Genome structure and expression

    Genome structure and expression

    Published 2009
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  4. 4
    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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  5. 5
    Copy number variation in mental retardation

    Copy number variation in mental retardation

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  6. 6
    Copy number variation in neuropsychiatric disorders

    Copy number variation in neuropsychiatric disorders

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  7. 7
    Databases for CNV in control and disease populations

    Databases for CNV in control and disease populations

    Published 2009
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  8. 8
    Indels, CNVs and the spectrum of human genome variation

    Indels, CNVs and the spectrum of human genome variation

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  9. 9
    CNVs and clinical diagnosis

    CNVs and clinical diagnosis

    Published 2009
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  10. 10
    Copy number variation

    Copy number variation

    Published 2009
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  11. 11
    Genome structure and expression

    Genome structure and expression

    Published 2009
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  12. 12
    Copy number variation

    Copy number variation

    Published 2009
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  13. 13
    CNVs and clinical diagnosis

    CNVs and clinical diagnosis

    Published 2009
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  14. 14
    Genome structure and expression

    Genome structure and expression

    Published 2009
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  15. 15
    Copy number variation in association studies of human disease

    Copy number variation in association studies of human disease

    Published 2009
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  16. 16
    Population genetics of structural variation

    Population genetics of structural variation

    Published 2009
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  17. 17
    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 /

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  18. 18
    Structural variants and susceptibility to common human disorders

    Structural variants and susceptibility to common human disorders

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  19. 19
    CNVs in human genomes

    CNVs in human genomes

    Published 2009
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  20. 20
    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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