Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
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Tessadori, Federico (Hubrecht Institute-KNAW)
;
Duran, Karen (Utrecht University) ;
Knapp, Karen (University of Otago) ;
Fellner, Matthias (University of Otago) ;
Smithson, Sarah (University Hospitals Bristol and Weston NHS Foundation Trust) ;
Beleza Meireles, Ana (University Hospitals Bristol and Weston NHS Foundation Trust) ;
Elting, Mariet W. (Amsterdam UMC) ;
Waisfisz, Quinten (Amsterdam UMC) ;
O'Donnell-Luria, Anne (Manton Center for Orphan Disease Research) ;
Nowak, Catherine (Manton Center for Orphan Disease Research) ;
Douglas, Jessica (Manton Center for Orphan Disease Research) ;
Ronan, Anne (Clinical Genetics) ;
Brunet, Theresa (Helmholtz Zentrum München) ;
Kotzaeridou, Urania (Heidelberg University Hospital (Alemanya)) ;
Svihovec, Shayna (University of Colorado Anschutz Medical Campus) ;
Saenz, Margarita S. (University of Colorado Anschutz Medical Campus) ;
Thiffault, Isabelle (Children's Mercy Hospital) ;
Del Viso, Florencia (Children's Mercy Hospital) ;
Devine, Patrick (University of California) ;
Rego, Shannon (University of California) ;
Tenney, Jessica (University of California) ;
van Haeringen, Arie (Leiden University Medical Center) ;
Ruivenkamp, Claudia A.L. (Leiden University Medical Center) ;
Koene, Saskia (Leiden University Medical Center) ;
Robertson, Stephen P. (University of Otago) ;
Deshpande, Charulata (Guy's and St Thomas' NHS Foundation Trust) ;
Pfundt, Rolph (Radboud University Medical Centre) ;
Verbeek, Nienke (University Medical Centre Utrecht) ;
van de Kamp, Jiddeke M. (Boston Children's Hospital (Boston, Estats Units d'Amèrica)) ;
Weiss, Janneke M.M. (Radboud University Medical Centre) ;
Ruiz, Anna (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT)) ;
Gabau, Elisabeth (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT)) ;
Banne, Ehud (Kaplan Medical Center) ;
Pepler, Alexander (Praxis für Humangenetik Tübingen) ;
Bottani, Armand (Geneva University Hospitals) ;
Laurent, Sacha (Geneva University Hospitals) ;
Guipponi, Michel (Geneva University Hospitals) ;
Bijlsma, Emilia (Leiden University Medical Center) ;
Bruel, Ange-Line (Dijon Bourgogne University Hospital) ;
Sorlin, Arthur (Dijon Bourgogne University Hospital) ;
Willis, Mary (Naval Medical Center San Diego) ;
Powis, Zoe (Ambry Genetics) ;
Smol, Thomas (Institut de Génétique Médicale) ;
Vincent-Delorme, Catherine (CHU Lille) ;
Baralle, Diana (University of Southampton) ;
Colin, Estelle (CHU d'Angers) ;
Revencu, Nicole (Université Catholique de Louvain) ;
Calpena, Eduardo (University of Oxford) ;
Wilkie, Andrew O.M. (University of Oxford) ;
Chopra, Maya (Boston Children's Hospital (Boston, Estats Units d'Amèrica)) ;
Cormier-Daire, Valerie (Université de Paris) ;
Keren, Boris (Pitié-Salpêtrière Hospital) ;
Afenjar, Alexandra (Sorbonne Université) ;
Niceta, Marcello (Ospedale Pediatrico Bambino Gesù (Roma, Itàlia)) ;
Terracciano, Alessandra (Ospedale Pediatrico Bambino Gesù (Roma, Itàlia)) ;
Specchio, Nicola (Ospedale Pediatrico Bambino Gesù (Roma, Itàlia)) ;
Tartaglia, Marco (Ospedale Pediatrico Bambino Gesù) ;
Rio, Marlene (Paris Descartes-Sorbonne Paris Cité University) ;
Barcia, Giulia (Paris Descartes-Sorbonne Paris Cité University) ;
Rondeau, Sophie (Paris Descartes-Sorbonne Paris Cité University) ;
Colson, Cindy (CHU Lille) ;
Bakkers, Jeroen (University Medical Center Utrecht) ;
Mace, Peter D. (University of Otago) ;
Bicknell, Louise S. (University of Otago) ;
van Haaften, Gijs (University Medical Center Utrecht) ;
Universitat Autònoma de Barcelona
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