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. 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x

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© de Munnik et al. 2015

Open Access This 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 — Facial features of Meier-Gorlin syndrome. Patient A is a girl aged 7 years and 9 months with two mutations in ORC4. Patient B is a 14 year old girl, who carries one mutation in ORC1. Both show the characteristic facial features of MGS, including microtia, a prominent nose with a convex nasal profile, a small mouth with full lips, and retro-/micrognathia