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Comment
. 2022 Dec;30(12):1318-1319.
doi: 10.1038/s41431-022-01174-y. Epub 2022 Aug 31.

Rare autosomal trisomies detected by non-invasive prenatal testing

Peter Benn  1
Affiliations
Comment

Rare autosomal trisomies detected by non-invasive prenatal testing

Peter Benn. Eur J Hum Genet. 2022 Dec.
No abstract available

PubMed Disclaimer

Conflict of interest statement

PB is a consultant and holds stock options in Natera, Inc. He is also on an Advisory Board for Menarini Biomarkers.

Comment on

References

    1. Lannoo L, van Straaten K, Breckot J, Brison N, de Catte L, Dimitriadou E, et al. Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge. Eur J Hum Genet. 2022. In press. - PMC - PubMed
    1. Benn P. Prenatal diagnosis of chromosome abnormalities through chorionic villus sampling and amniocentesis. 8th ed. Chichester, England: Wiley Blackwell; 2021.
    1. Fragouli E, Munne S, Wells D. The cytogenetic constitution of human blastocysts: insights from comprehensive chromosome screening strategies. Hum Reprod Update. 2019;25:15–33. doi: 10.1093/humupd/dmy036. - DOI - PubMed
    1. Benn P, Grati FR. Aneuploidy in first trimester chorionic villi and spontaneous abortions: windows into the origin and fate of aneuploidy through embryonic and fetal development. Prenat Diagn. 2021;41:519–24. doi: 10.1002/pd.5795. - DOI - PubMed
    1. Toutain J, Goutte-Gattat D, Horovitz J, Saura R. Confined placental mosaicism revisited: impact on pregnancy characteristics and outcome. PloS One. 2018;13:e0195905. doi: 10.1371/journal.pone.0195905. - DOI - PMC - PubMed