Heterozygous variants in <scp><i>ZBTB7A</i></scp> cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin
Charlotte von der Lippe(Telemark Hospital), Wenche Moe Thorstensen(Norwegian University of Science and Technology), Ana S.A. Cohen(Children's Mercy Hospital), Stephen Jolles(University Hospital of Wales), Øystein L. Holla(Telemark Hospital), Salvador Climent(Istinye University), Jonathan Lévy(Assistance Publique – Hôpitaux de Paris), Janet Hoenicka(Hospital Sant Joan de Déu Barcelona), Andrew E. Fry(University Hospital of Wales), Nicolas Derive, Kristian Tveten(Telemark Hospital), Irene Bruno(IRCCS Materno Infantile Burlo Garofolo), Shivarajan Amudhavalli(Children's Mercy Hospital), Carol Macmillan(University of Chicago), Frédérique Bonnet‐Brilhault(Inserm), Séverine Drunat(Délégation Paris 7), Øyvind L. Busk(Telemark Hospital), Deborah Osio(Birmingham Women's Hospital), Júlia Baptista(University of Exeter), Marte G. Haug(St Olav's University Hospital), Francis H. Sansbury(Ninewells Hospital), Flavio Faletra(IRCCS Materno Infantile Burlo Garofolo), Katherine Burke(University of Alabama), Francesc Palau(Hospital Sant Joan de Déu Barcelona), Trine Prescott(Telemark Hospital), Derek Lim(Birmingham Women’s and Children’s NHS Foundation Trust), Roser Urreitzi(Centre for Biomedical Network Research on Rare Diseases), Kendra Engleman(Children's Mercy Hospital), Médéric Jeanne(Boston Children's Hospital), Jennifer Evans(Kwame Nkrumah University of Science and Technology), Dihong Zhou(Children's Mercy Hospital)
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