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. 2014 Jun 4;6(1):11. doi: 10.1186/1868-7083-6-11

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Copyright © 2014 Ibrahim et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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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Frequencies of Beckwith-Wiedemann syndrome clinical features according to molecular subtype. (a) Hemihypertrophy, (b) macroglossia, (c) facial naevus flammeus, (d) ear creases/pits, (e) exomphalos, (f) organomegaly, and (g) embryonal tumours. ALL-MUT, all mutations; IC1, imprinting centre 1; IC2, imprinting centre 2; NIL, no mutations; pUPD, paternal uniparental disomy.