Review



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


Bioz Verified Symbol Agilent technologies is a verified supplier
Bioz Manufacturer Symbol Agilent technologies manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    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/result/high-resolution custom array comparative genomic hybridization (cgh/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    high-resolution custom array comparative genomic hybridization (cgh - by Bioz Stars, 2026-05
    90/100 stars

    Images

    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:



    Similar Products

    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/result/high-resolution custom array comparative genomic hybridization (cgh/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    high-resolution custom array comparative genomic hybridization (cgh - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    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: