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custom high-definition dna comparative genomic hybridization arrays 8×15 k  (Agilent technologies)


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    Agilent technologies custom high-definition dna comparative genomic hybridization arrays 8×15 k
    Custom High Definition Dna Comparative Genomic Hybridization Arrays 8×15 K, 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/result/custom high-definition dna comparative genomic hybridization arrays 8×15 k/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    custom high-definition dna comparative genomic hybridization arrays 8×15 k - by Bioz Stars, 2026-04
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    high-resolution custom array comparative genomic hybridization (cgh  (Agilent technologies)
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    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>
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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.).

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