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Comment
. 2024 Nov;44(12):1498-1499.
doi: 10.1002/pd.6655. Epub 2024 Sep 14.

Correspondence on "Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"

Julia Wynn  1 , Jennifer Hoskovec  1
Affiliations
Comment

Correspondence on "Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"

Julia Wynn et al. Prenat Diagn. 2024 Nov.
No abstract available

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References

    1. N. L. Vora, S. Langlois, and L. S. Chitty, “Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use,” Prenatal Diagnosis 44, no. 4 (2024): 389–397, PMID: 37991340, https://doi.org/10.1002/pd.6469.
    1. D. S. Tsao, S. Silas, B. P. Landry, et al., “A Novel High‐Throughput Molecular Counting Method With Single Base‐Pair Resolution Enables Accurate Single‐Gene NIPT,” Scientific Reports 9, no. 1 (2019): 14382, https://doi.org/10.1038/S41598‐019‐50378‐8.
    1. J. Hoskovec, E. E. Hardisty, A. N. Talati, et al., “Maternal Carrier Screening With Single‐Gene NIPS Provides Accurate Fetal Risk Assessments for Recessive Conditions,” Genetics in Medicine 25, no. 2 (2022): 1–103, https://doi.org/10.1016/j.gim.2022.10.014.
    1. J. Wynn, J. Hoskovec, R. D. Carter, M. J. Ross, and S. C. Perni, “Performance of Single‐Gene Noninvasive Prenatal Testing for Autosomal Recessive Conditions in a General Population Setting,” Prenatal Diagnosis 43, no. 10 (2023): 1344–1354, https://doi.org/10.1002/PD.6427.
    1. R. Ben‐Shachar, A. Svenson, J. D. Goldberg, and D. Muzzey, “A Data‐Driven Evaluation of the Size and Content of Expanded Carrier Screening Panels,” Genetics in Medicine 21, no. 9 (2019): 1931–1939, PMID: 30816298; PMCID: PMC6752311, https://doi.org/10.1038/s41436‐019‐0466‐5.

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