Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study

Author(s):
Opstal, D. van; Maarle, M.C. van; Lichtenbelt, K.; Weiss, M.M.; Schuring-Blom, H.; Bhola, S.L.; Hoffer, M.J.V. (0000-0002-1812-7670); Huijsdens-van Amsterdam, K.; Macville, M.V.; Kooper, A.J.A.; Faas, B.H.W.; Govaerts, L.; Tan-Sindhunata, G.M.; Hollander, N. den; Feenstra, I.; Galjaard, R.J.H.; Oepkes, D.; Ghesquiere, S.; Brouwer, R.W.W.; Beulen, L.; Bollen, S.; Elferink, M.G.; Straver, R.; Henneman, L.; Page-Christiaens, G.C.; Sistermans, E.A.; Dutch NIPT Consortium
Published
2018
Publication type
Article / Letter to editor
confined placental mosaicismgenome-wide NIPSnoninvasive testingprenatal screeningtrisomy 21
Date issued
2018-05-31
Language
English
Is part of
Genetics in Medicine (2018), Vol. 20, no. 5, p. 480-485
hdl
1887/79425
doi
10.1038/gim.2017.132
URL
https://www.nature.com/articles/gim2017132.pdf