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    • ACMG Statements and Guidelines
    • Driscoll, Deborah ARemove Driscoll, Deborah A filter
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    • Research Article6

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    • Gross, Susan J3
    • Pletcher, Beth A2
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    • Genetics in Medicine6

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    • aneuploidy3
    • multiple marker screening3
    • nuchal translucency2
    • FMR11
    • fragile X syndrome1
    • genetic evaluation1
    • genetic referral1
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    ACMG Statements and Guidelines

    These online statements and guidelines are definitive and may be cited using the digital object identifier (DOI). These recommendations are designed primarily as an educational resource for medical geneticists and other healthcare providers to help them provide quality medical genetics services; they should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. Please refer to the leading disclaimer in each document for more information.

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    • ACMG Practice Guidelines
      Open Archive

      Screening for fetal aneuploidy and neural tube defects

      Genetics in Medicine
      Vol. 11Issue 11p818–821Published in issue: November, 2009
      • Deborah A. Driscoll
      • Susan J. Gross
      • for the Professional Practice Guidelines Committee
      Cited in Scopus: 63
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        Maternal serum screening for neural tube defects and fetal aneuploidy in the second trimester has been incorporated into obstetrical practice over the past two decades. Now, as a result of several multicenter trials, first trimester screening between 11 and 14 weeks has been shown to be an effective and reliable screening test for Down syndrome and trisomy 18. This policy updates the American College of Medical Genetics policy statement entitled Second Trimester Maternal Serum Screening for Fetal Open Neural Tube Defects and Aneuploidy (2004), incorporates First trimester diagnosis and screening for fetal aneuploidy (2008) and complements the sections of American College of Medical Genetic's Standards and Guidelines for Clinical Genetics Laboratories entitled Prenatal Screening for Down syndrome (2005) and Prenatal Screening for Open Neural Tube Defects (2005).
      • ACMG-Practice-Guidelines
        Open Archive

        First trimester diagnosis and screening for fetal aneuploidy

        Genetics in Medicine
        Vol. 10Issue 1p73–75Published in issue: January, 2008
        • Deborah A. Driscoll
        • Susan J. Gross
        • for the Professional Practice and Guidelines Committee
        Cited in Scopus: 44
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          Maternal serum screening for neural tube defects and fetal aneuploidy in the second trimester has been incorporated into obstetrical practice over the past two decades. Now, as a result of several multicenter trials, first trimester screening between 11 and 14 weeks has been shown to be an effective and reliable screening test for Down syndrome and trisomy 18. Benefits of first trimester screening include earlier identification of the pregnancy at risk for fetal aneuploidy and anatomic defects, in particular, cardiac anomalies, and the option of earlier diagnosis by chorionic villus sampling, if available.
        • ACMG Practice Guidelines
          Open Archive

          Indications for genetic referral: a guide for healthcare providers

          Genetics in Medicine
          Vol. 9Issue 6p385–389Published in issue: June, 2007
          • Beth A. Pletcher
          • Helga V. Toriello
          • Sarah J. Noblin
          • Laurie H. Seaver
          • Deborah A. Driscoll
          • Robin L. Bennett
          • and others
          Cited in Scopus: 40
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            Disclaimer: This guideline is designed primarily as an educational resource for medical geneticists and other healthcare providers to help them provide quality medical genetic services. Adherence to this guideline does not necessarily assure a successful medical outcome. This guideline should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, the geneticist should apply his or her own professional judgment to the specific clinical circumstances presented by the individual patient or specimen.
          • ACMG Standards and Guidelines
            Open Archive

            Fragile X syndrome: Diagnostic and carrier testing

            Genetics in Medicine
            Vol. 7Issue 8p584–587Published in issue: October, 2005
            • Stephanie Sherman
            • Beth A. Pletcher
            • Deborah A. Driscoll
            Cited in Scopus: 229
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              Disclaimer: This guideline is designed primarily as an educational resource for medical geneticists and other health care providers to help them provide quality medical genetic services. Adherence to this guideline does not necessarily assure a successful medical outcome. This guideline should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, the geneticist should apply his or her own professional judgment to the specific clinical circumstances presented by the individual patient or specimen.
            • ACMG Practice Guidelines
              Open Archive

              Second trimester maternal serum screening for fetal open neural tube defects and aneuploidy

              Genetics in Medicine
              Vol. 6Issue 6p540–541Published in issue: November, 2004
              • Deborah A. Driscoll
              Cited in Scopus: 14
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                Maternal serum screening has been modified during the past 25 years and is now widely utilized during the second trimester to identify women at risk for fetal open neural tube defects (ONTDs), anencephaly, and trisomies 21 and 18. This statement replaces the 1994 and 1996 ACMG position statements on serum screening and discusses clinical guidelines for screening that complement the sections of ACMG’s Standards and Guidelines for Clinical Genetics Laboratories entitled “Prenatal screening for open neural tube defects” and “Prenatal screening for Down syndrome” ( http://www.acmg.net ).
              • ACMG Policy Statement
                Open Archive

                Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

                Genetics in Medicine
                Vol. 6Issue 5p387–391Published in issue: September, 2004
                • Michael S. Watson
                • Garry R. Cutting
                • Robert J. Desnick
                • Deborah A. Driscoll
                • Katherine Klinger
                • Michael Mennuti
                • and others
                Cited in Scopus: 368
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                  An erratum to this article is available online at https://doi.org/10.1038/gim200480 .
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