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Mutations in TBL1X as a Novel Cause of Familial Central Hypothyroidism | ESPE2016
Charlotte Heinen; Monique Losekoot; Yu Sun; Peter Watson; Louise Fairall; Sjoerd Joustra; Nitash Zwaveling-Soonawala; Wilma Oost
http://abstracts.eurospe.org/hrp/0086/hrp0086fc11.1.htm
Published: 2016-08-19

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Paternally Inherited IGF2 Mutation Results in Intrauterine and Postnatal Growth Retardation | ESPE2015
Matthias Begemann; Birgit Zirn; Gijs Santen; Elisa Wirthgen; Lukas Soellner; Hans-Martin Buttel; Roland Schweizer; Workum Wilber
http://abstracts.eurospe.org/hrp/0084/hrp0084fc-lb-5.htm
Published: 2015-08-26

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