Škorić-Milosavljević, Doris
Lahrouchi, Najim
Bosada, Fernanda M.
Dombrowsky, Gregor
Williams, Simon G.
Lesurf, Robert
Tjong, Fleur V.Y.
Walsh, Roddy
El Bouchikhi, Ihssane
Breckpot, Jeroen
Audain, Enrique
Ilgun, Aho
Beekman, Leander
Ratbi, Ilham
Strong, Alanna
Muenke, Maximilian
Heide, Solveig
Muir, Alison M.
Hababa, Mariam
Cross, Laura
Zhou, Dihong
Pastinen, Tomi
Hitz, Marc-Phillip
Abdul-Khaliq, Hashim
Berger, Felix
Dähnert, Ingo
Dittrich, Sven
Uebing, Anselm
Stiller, Brigitte
Zackai, Elaine
Atmani, Samir
Ouldim, Karim
Adadi, Najlae
Steindl, Katharina
Rauch, Anita
Brook, David
Wilsdon, Anna
Kuipers, Irene
Blom, Nico A.
Mulder, Barbara J.
Mefford, Heather C.
Keren, Boris
Joset, Pascal
Kruszka, Paul
Thiffault, Isabelle
Sheppard, Sarah E.
Roberts, Amy
Lodder, Elisabeth M.
Keavney, Bernard D.
Clur, Sally-Ann B.
Mital, Seema
Hitz, Marc-Philip
Christoffels, Vincent M.
Postma, Alex V.
Bezzina, Connie R.
This article is maintained by: Elsevier
Article Title: Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01279-7
CrossRef DOI link to the associated document: https://doi.org/10.1038/s41436-021-01212-y
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics