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high-resolution custom array comparative genomic hybridization (cgh  (Agilent technologies)


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    Agilent technologies high-resolution custom array comparative genomic hybridization (cgh
    Pedigrees <t>of</t> <t>15q13.3</t> microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by <t>array-CGH.</t>
    High Resolution Custom Array Comparative Genomic Hybridization (Cgh, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/high-resolution+custom+array+comparative+genomic+hybridization+(cgh/pmc03270691-20-19-41
    Average 90 stars, based on 1 article reviews
    high-resolution custom array comparative genomic hybridization (cgh - by Bioz Stars, 2026-10
    90/100 stars

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    1) Product Images from "Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome"

    Article Title: Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome

    Journal: Epilepsia

    doi: 10.1111/j.1528-1167.2011.03301.x

    Pedigrees of 15q13.3 microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by array-CGH.
    Figure Legend Snippet: Pedigrees of 15q13.3 microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by array-CGH.

    Techniques Used:

    Related Articles

    Refining:

    Article Title: Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome
    Article Snippet: Confirmation of 15q13.3 microdeletions and refining of the breakpoints in probands and screening of family members was performed using high-resolution custom array comparative genomic hybridization (CGH) with 4,398 probes in the 15q13 BP3-BP5 region (hg18, chr15:26,500,000–31,000,000; average probe spacing 1,250 bp; Agilent Technologies, Santa Clara, CA, U.S.A.).

    Hybridization:

    Article Title: Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome
    Article Snippet: Confirmation of 15q13.3 microdeletions and refining of the breakpoints in probands and screening of family members was performed using high-resolution custom array comparative genomic hybridization (CGH) with 4,398 probes in the 15q13 BP3-BP5 region (hg18, chr15:26,500,000–31,000,000; average probe spacing 1,250 bp; Agilent Technologies, Santa Clara, CA, U.S.A.).



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    high-resolution custom array comparative genomic hybridization (cgh  (Agilent technologies)
    90
    Agilent technologies high-resolution custom array comparative genomic hybridization (cgh
    Pedigrees <t>of</t> <t>15q13.3</t> microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by <t>array-CGH.</t>
    High Resolution Custom Array Comparative Genomic Hybridization (Cgh, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/high-resolution+custom+array+comparative+genomic+hybridization+(cgh/pmc03270691-20-19-41
    Average 90 stars, based on 1 article reviews
    high-resolution custom array comparative genomic hybridization (cgh - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

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    Pedigrees of 15q13.3 microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by array-CGH.

    Journal: Epilepsia

    Article Title: Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome

    doi: 10.1111/j.1528-1167.2011.03301.x

    Figure Lengend Snippet: Pedigrees of 15q13.3 microdeletion carriers. All four probands (marked by the arrow) are affected by absence seizures and intellectual disability. Additional microdeletion carriers (family of proband 1) are marked by an asterisk. No deletions (“no del”) were found in several relatives investigated by array-CGH.

    Article Snippet: Confirmation of 15q13.3 microdeletions and refining of the breakpoints in probands and screening of family members was performed using high-resolution custom array comparative genomic hybridization (CGH) with 4,398 probes in the 15q13 BP3-BP5 region (hg18, chr15:26,500,000–31,000,000; average probe spacing 1,250 bp; Agilent Technologies, Santa Clara, CA, U.S.A.).

    Techniques: