Courraud, Julie
Russo, Francesco http://orcid.org/0000-0001-9257-4359
Themudo, Gonçalo Espregueira http://orcid.org/0000-0002-5019-9439
Laursen, Susan Svane
Ingason, Andrés
Hougaard, David M. http://orcid.org/0000-0001-5928-3517
Cohen, Arieh S.
Werge, Thomas http://orcid.org/0000-0003-1829-0766
Ernst, Madeleine http://orcid.org/0000-0001-9530-3837
Funding for this research was provided by:
Lundbeckfonden (R102-A9118, R155-2014-1724, R268-2016-3925, R102-A9118, R155-2014-1724, R268-2016-3925, R102-A9118, R155-2014-1724, R268-2016-3925, R155-2014-1724, R268-2016-3925, R102-A9118, R155-2014-1724, R102-A9118, R155-2014-1724)
Article History
Received: 20 January 2023
Revised: 22 November 2023
Accepted: 29 November 2023
First Online: 14 December 2023
Competing interests
: The authors declare no competing interests.
: The scientific board of the Danish Cytogenetic Central Register approved the study and provided access to the genetic data that provided information on individuals with a 22q11.2 deletion and was obtained from the Danish Cytogenetic Central Registry (DCCR), which was established in 1968 and contains data on every karyotype obtained by clinical departments performing chromosomal analyses in Denmark. The project was approved by the scientific ethics committees (Videnskabsetiske Komitéer, Reg. nr: H-B-2009-026) and the Danish Data Protection Agency (Datatilsynet, Reg. nr: 2007-58-0015).