De novo variants in <scp><i>TCF7L2</i></scp> are associated with a syndromic neurodevelopmental disorder
Caroline Dias(University of Colorado Anschutz Medical Campus), Lance H. Rodan(Boston Children's Hospital), Christopher A. Walsh(Boston Children's Hospital), Rolph Pfundt(Radboud University Nijmegen), Maria Iascone(Ospedale Papa Giovanni XXIII), François Lecoquierre(Inserm), Silvia Maitz(Azienda Ospedaliera San Gerardo), Petra Zwijnenburg(Hospitais da Universidade de Coimbra), Tova Hershkovitz(Bar-Ilan University), Marjan M. Weiss(Radboud University Nijmegen), Tawfeg Ben‐Omran(Qatar Airways (Qatar)), Lynn Pais(MACOM (United States)), Aude Charollais(Université de Rouen Normandie), Karin Weiss(Technion – Israel Institute of Technology), Jennifer A. Sullivan(Duke Medical Center), Nicholas Stong(New York Genome Center), René G. Feichtinger(Paracelsus Medical University), Dieter Kotzot(Paracelsus Medical University), Johannes A. Mayr(Paracelsus Medical University), Cyril Mignot(Sorbonne Université), Vandana Shashi(University of Virginia Medical Center), Anne‐Marie Guerrot(Inserm), Tjitske Kleefstra(Radboud University Nijmegen), Janneke Shuurs-Hoeijmakers(Radboud University Nijmegen), Elles M. J. Boon(Amsterdam University Medical Centers), Arnaud Isapof(Sorbonne Université), Laila Mahmoud(Hamad Medical Corporation), Johanna M. van Hagen(Amsterdam University Medical Centers), Boris Keren(Sorbonne Université)
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