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. 2021 Jul 27;2021(3):hoab024. doi: 10.1093/hropen/hoab024

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© The Author(s) 2021. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Distribution of PGT indications in 2016–2017. (A) Pre-implantation testing for monogenic/single gene defects (PGT-M), (B) PGT for chromosomal structural rearrangements (PGT-SR), (C) PGT for aneuploidies (PGT-A) and (D) concurrent PGT-M/SR with PGT-A. AD, autosomal dominant; AR, autosomal recessive; XL-D, X-linked dominant; XL-R, X-linked recessive; AMA, advanced maternal age; Rec misc, recurrent miscarriage; RIF, repeated implantation failure; Prev abnormal pregn, previous abnormal pregnancy.