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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.
2 Results
- ACMG Systematic Evidence Review
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies
Genetics in MedicineVol. 24Issue 7p1379–1391Published online: May 24, 2022- Nancy C. Rose
- Elizabeth S. Barrie
- Jennifer Malinowski
- Gabrielle P. Jenkins
- Monica R. McClain
- Danielle LaGrave
- and others
Cited in Scopus: 7Noninvasive prenatal screening (NIPS) using cell-free DNA has been assimilated into prenatal care. Prior studies examined clinical validity and technical performance in high-risk populations. This systematic evidence review evaluates NIPS performance in a general-risk population. - AddendumOpen Archive
Addendum: Technical standards and guidelines: Molecular genetic testing for ultra-rare disorders
Genetics in MedicineVol. 24Issue 1p253–253.e1Published online: November 30, 2021- Caroline Astbury
- Judith Benkendorf
- ACMG Laboratory Quality Assurance Committee
Cited in Scopus: 0This document was retired by the American College of Medical Genetics and Genomics (ACMG) Board of Directors as of May 20, 2019 with the following addendum.