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- Andersen, Erica F1
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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.
3 Results
- CorrectionOpen Archive
Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)
Genetics in MedicineVol. 23Issue 11p2230Published in issue: November, 2021- Erin Rooney Riggs
- Erica F. Andersen
- Athena M. Cherry
- Sibel Kantarci
- Hutton Kearney
- Ankita Patel
- and others
Cited in Scopus: 7The original article can be found online at https://doi.org/10.1038/s41436-019-0686-8 . - CorrectionOpen Archive
Correction: Addendum: ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing
Genetics in MedicineVol. 22Issue 9p1568Published in issue: September, 2020- Michael T. Bashford
- Scott E. Hickey
- Cynthia J. Curry
- Helga V. Toriello
Cited in Scopus: 0An amendment to this paper has been published and can be accessed via a link at the top of the paper. - ACMG Policy StatementOpen Archive
Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening
Genetics in MedicineVol. 2Issue 2p149–150Published in issue: March, 2000- Walter E. Nance
- George C. Cunningham
- Jessica G. Davis
- Cynthia C. Morton
- Louis J. Elsas
- Teresa Finitzo
- and others
Cited in Scopus: 14
