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. 2016 Jan 12;9:3. doi: 10.1186/s13039-016-0213-4

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© Wang et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Genetic testing of fetus and her parents. a a partial deletion in chromosome 13 was detected by NIPT; b a partial deletion in chromosome 21 was detected by NIPT; c about 22.0 Mb deletions in q31.3-q34 of chromosome 13 was validated by aCGH; d about 16.0 Mb deletions in q11.1-q21.3 of chromosome 21 was validated by aCGH; e the fetal karyotype was 45,XX, der(13),-21; f the maternal karyotype was 46,XX,inv(9)(p12q13),t(13;21)(q31.3;q21.3)