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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8)

Erin Rooney Riggs; Erica F. Andersen; Athena M. Cherry; Sibel Kantarci; Hutton Kearney; Ankita Patel; Gordana Raca; Deborah I. Ritter; Sarah T. South; Erik C. Thorland; Daniel Pineda-Alvarez; Swaroop Aradhya; Christa Lese Martin

doi:10.1038/s41436-021-01150-9

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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8)

Erin Rooney Riggs, Erica F. Andersen, Athena M. Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I. Ritter, Sarah T. South, Erik C. Thorland, Daniel Pineda-Alvarez, Swaroop Aradhya, Christa Lese Martin

Laboratory Medicine and Pathology

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

A Correction to this paper has been published: https://doi.org/10.1038/s41436-021-01150-9.

Original language	English (US)
Pages (from-to)	2230
Number of pages	1
Journal	Genetics in Medicine
Volume	23
Issue number	11
DOIs	https://doi.org/10.1038/s41436-021-01150-9
State	Published - Nov 2021

ASJC Scopus subject areas

Genetics(clinical)

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Riggs, E. R., Andersen, E. F., Cherry, A. M., Kantarci, S., Kearney, H., Patel, A., Raca, G., Ritter, D. I., South, S. T., Thorland, E. C., Pineda-Alvarez, D., Aradhya, S., & Martin, C. L. (2021). 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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8). Genetics in Medicine, 23(11), 2230. https://doi.org/10.1038/s41436-021-01150-9

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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8). / Riggs, Erin Rooney; Andersen, Erica F.; Cherry, Athena M. et al.
In: Genetics in Medicine, Vol. 23, No. 11, 11.2021, p. 2230.

Research output: Contribution to journal › Comment/debate › peer-review

Riggs, ER, Andersen, EF, Cherry, AM, Kantarci, S, Kearney, H, Patel, A, Raca, G, Ritter, DI, South, ST, Thorland, EC, Pineda-Alvarez, D, Aradhya, S & Martin, CL 2021, '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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8)', Genetics in Medicine, vol. 23, no. 11, pp. 2230. https://doi.org/10.1038/s41436-021-01150-9

Riggs ER, Andersen EF, Cherry AM, Kantarci S, Kearney H, Patel A et al. 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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8). Genetics in Medicine. 2021 Nov;23(11):2230. doi: 10.1038/s41436-021-01150-9

Riggs, Erin Rooney ; Andersen, Erica F. ; Cherry, Athena M. et al. / 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 Medicine, (2020), 22, 2, (245-257), 10.1038/s41436-019-0686-8). In: Genetics in Medicine. 2021 ; Vol. 23, No. 11. pp. 2230.

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Abstract

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