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. 2020 Jun 16;4(12):bvaa071. doi: 10.1210/jendso/bvaa071

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© The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Pedigrees of A, family 1 and B, family 2, highlighting succinate dehydrogenase (SDH)-related and other tumors in affected family members. Genetic status regarding the intronic SDHC variant c.20 + 74A >G is indicated in the top right-hand corner for all tested individuals. ⁺, variant present; ^–, variant absent.