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Addendum: Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

  • Melanie Manning
    Affiliations
    Department of Pathology, Stanford University School of Medicine Stanford CA USA

    Department of Pediatrics; Pediatrics, Stanford University School of Medicine Stanford CA USA
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  • Louanne Hudgins
    Affiliations
    Department of Pathology, Stanford University School of Medicine Stanford CA USA

    American College of Medical Genetics and Genomics Bethesda MD USA
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  • The American College of Medical Genetics and Genomics (ACMG) Professional Practice and Guidelines Committee
    *
      Addendum to: Genetics in Medicine 12:742–745 (2010) https://doi.org/10.1097/GIM.0b013e3181f8baad, published online 18 October 2010.
      This document was reaffirmed by the ACMG Board of Directors as of 27 April 2020 with the following addendum:
      We suggest the following considerations in reaffirming this document:
      • 1.
        Since this document no longer meets the criteria for an evidence-based practice guideline by the College, it has been reclassified as a Clinical Practice Resource.
      • 2.
        Technical information for array-based testing may be referenced at the ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.
        • Working Group for the American College of Medical Genetics and Genomics Laboratory Quality Assurance Committee.
        ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

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      Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

      Reference

        • Working Group for the American College of Medical Genetics and Genomics Laboratory Quality Assurance Committee.
        ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.
        1:CAS:528:DC%2BC3sXhslGntLvI
        10.1038/gim.2013.129
        Genet Med. 2013; 15: 901-909