Konrad, Enrico D.H.
Nardini, Niels
Caliebe, Almuth
Nagel, Inga
Young, Dana
Horvath, Gabriella
Santoro, Stephanie L.
Shuss, Christine
Ziegler, Alban
Bonneau, Dominique
Kempers, Marlies
Pfundt, Rolph
Legius, Eric
Bouman, Arjan
Stuurman, Kyra E.
Õunap, Katrin
Pajusalu, Sander
Wojcik, Monica H.
Vasileiou, Georgia
Le Guyader, Gwenaël
Schnelle, Hege M.
Berland, Siren
Zonneveld-Huijssoon, Evelien
Kersten, Simone
Gupta, Aditi
Blackburn, Patrick R.
Ellingson, Marissa S.
Ferber, Matthew J.
Dhamija, Radhika
Klee, Eric W.
McEntagart, Meriel
Lichtenbelt, Klaske D.
Kenney, Amy
Vergano, Samantha A.
Abou Jamra, Rami
Platzer, Konrad
Ella Pierpont, Mary
Khattar, Divya
Hopkin, Robert J.
Martin, Richard J.
Jongmans, Marjolijn C.J.
Chang, Vivian Y.
Martinez-Agosto, Julian A.
Kuismin, Outi
Kurki, Mitja I.
Pietiläinen, Olli
Palotie, Aarno
Maarup, Timothy J.
Johnson, Diana S.
Venborg Pedersen, Katja
Laulund, Lone W.
Lynch, Sally A.
Blyth, Moira
Prescott, Katrina
Canham, Natalie
Ibitoye, Rita
Brilstra, Eva H.
Shinawi, Marwan
Fassi, Emily
Sticht, Heinrich
Gregor, Anne
Van Esch, Hilde
Zweier, Christiane
Funding for this research was provided by:
Deutsche Forschungsgemeinschaft (ZW184/1-2)
Deutsche Forschungsgemeinschaft (ZW184/3-1)
Deutsche Forschungsgemeinschaft (270949263/GRK2162)
IZKF, Medizinische Fakultät, Friedrich-Alexander-Universität Erlangen-Nürnberg (E26)
FWO Vlaanderen (0000)
Wellcome Trust (WT098051)
Health Innovation Challenge Fund (HICF-1009-003)
National Human Genome Research Institute (UM1 HG008900)
Estonian Research Council (PUT355)
Estonian Research Council (PRG471)
Estonian Research Council (PUTJD827)
National Institutes of Health (T32GM007748)
ELAN-Fonds, FAU Erlangen-Nürnberg (0000)
This article is maintained by: Elsevier
Article Title: CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0585-z
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics