Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi(Columbia University Irving Medical Center), Elizabeth Bhoj(Children's Hospital of Philadelphia), Elaine H. Zackai(Children's Hospital of Philadelphia), Florence Démurger(Centre hospitalier Bretagne Atlantique), Nuria C. Bramswig(Düsseldorf University Hospital), Wendy K. Chung, Michael March(Children's Hospital of Philadelphia), Leticia S. Matsuoka(Children's Hospital of Philadelphia), Stephanie Lucia(Boston Children's Hospital), Isabelle Thiffault(Children's Mercy Hospital), Ariane Schmetz(Düsseldorf University Hospital), Anshuman Sewda(Columbia University Irving Medical Center), Jeanne Amiel(Hôpital Necker-Enfants Malades), Maria Francesca Bedeschi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), John P. Schacht(Columbia University Irving Medical Center), Angela Peron(University of Milan), Priyanka Ahimaz(Columbia University Irving Medical Center), Alejandro Iglesias(Columbia University Irving Medical Center), Stephanie M. Baskin(Children's Mercy Hospital), Christopher T. Gordon(Délégation Paris 5), Bertrand Isidor(Centre National de la Recherche Scientifique), Sara Benito‐Sanz(Hospital Universitario La Paz), Susan M. White(The University of Melbourne), Katherine Lachlan(Salisbury District Hospital), Joan M. Stoler(Harvard University Press), Verónica Seidel(Boston Children's Hospital), Júlia Baptista(University of Exeter), Sarah Bowdin(University of Birmingham), Amanda Thomas‐Wilson(Columbia University Irving Medical Center), Dong Li(Children's Hospital of Philadelphia), Lisa Bastarache(Vanderbilt University Medical Center), Benjamin Cogné(Centre National de la Recherche Scientifique), Elly Brokamp(Vanderbilt University Medical Center), Jenny Morton(Birmingham Women's Hospital), Karen Stals(Royal Devon & Exeter NHS Foundation Trust)
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