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prejudicing the impartiality of this review. Funding S C and M C are supported by a grant from the Flanders Research Foundation (FWO grant G044119N). This publication has been supported by Endo-ERN, which is co-funded by the European Union’s 3rd Health
Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark
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Department of Clinical Genetics and Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark
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Unit for Thrombosis Research, Hospital of South West Jutland and University of Southern Denmark, Esbjerg, Denmark
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Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark
Unit for Thrombosis Research, Hospital of South West Jutland and University of Southern Denmark, Esbjerg, Denmark
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H Gravholt and Kirstine Stochholm are members of the European Reference Network on Rare Endocrine Conditions (ENDO-ERN), Project ID number 739543. References 1 Berglund A Viuff MH Skakkebæk A Chang S Stochholm K & Gravholt CH
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This publication has been supported by the European Reference Network on Rare Endocrine Conditions (Endo-ERN), which is co-funded by the European Union’s 3rd Health Program (CHAFEA Framework Partnership Agreement No. 739527). Author contribution