SLNSW-Detection of genomic copy number changes in patie...-TN_cdi_proquest_miscellaneous_68268320

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

Full title: Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

Author/creator: Froyen, Guy, Van Esch, Hilde, Bauters, Marijke, Hollanders, Karen, Frints, Suzanna G.M, Vermeesch, Joris R, Devriendt, Koen, Fryns, Jean-Pierre, Marynen, Peter.

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Record Identifier: TN_cdi_proquest_miscellaneous_68268320

Language: English

Formats: Articles

Publishers: Hoboken: Wiley Subscription Services, Inc., A Wiley Company

Permalink: https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68268320

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    Record title

    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

    Record identifier

    TN_cdi_proquest_miscellaneous_68268320

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68268320

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    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68268320

    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

    Full title

    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes

    Author / Creator

    Froyen, Guy ; Van Esch, Hilde ; Bauters, Marijke ; Hollanders, Karen ; Frints, Suzanna G.M ; Vermeesch, Joris R ; Devriendt, Koen ; Fryns, Jean-Pierre ; Marynen, Peter

    Publisher

    Hoboken: Wiley Subscription Services, Inc., A Wiley Company

    Journal title

    Human mutation, 2007, Vol.28 (10), p.1034-1042

    Record Identifier

    TN_cdi_proquest_miscellaneous_68268320

    Language

    English

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    Subjects and topics

    Adolescent array‐CGH Child Child, Preschool Chromosomes, Human, X duplication Female Gene Deletion Gene Dosage Genetic Linkage Genome Genotype genotype–phenotype Humans Intellectual Disability - genetics Male mental retardation Nucleic Acid Hybridization Phenotype X‐linked

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    TN_cdi_proquest_miscellaneous_68268320

    Permalink

    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68268320

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