Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Andrew K. Sobering(St. George's University), Elizabeth Bhoj(Children's Hospital of Philadelphia), Arie van Haeringen(Leiden University), Roos Cuperus, Jessica Douglas(Boston University), Julie Vogt(Birmingham Women's Hospital), Anne Chun‐Hui Tsai(University of Oklahoma Health Sciences Center), Stanislas Lyonnet(Hôpital Necker-Enfants Malades), Sandrine Marlin, John M. Graham(Cedars-Sinai Medical Center), Julie McGaughran(St Mary's Hospital), Aida Telegrafi(GenVec), Helen V. Firth(Royal Devon and Exeter Hospital), Dawn Earl(Seattle Children's Hospital), Laura Bryant(Penn Presbyterian Medical Center), Oleksandra Petryna(Ocean Medical Center), Alban Ziegler(Columbia University Irving Medical Center), Michael J. Bamshad(University of Utah), Beverly P. Nelson, Jane Juusola, Brandon Alexander Holt(St. George's University), Stéphanie Moortgat(Institute of Pathology and Genetics), Jacob Zyskind(ID Genomics (United States)), Claudia Ruivenkamp(The Netherlands Cancer Institute), Véronique Pingault(Institut des Maladies Génétiques Imagine), Isabelle Maystadt(Institute of Pathology and Genetics), Kirsty McWalter, Maria Steenhof(Odense University Hospital), Charlotte Brasch‐Andersen(University of Southern Denmark), Dong Li(Children's Hospital of Philadelphia), Jenny Morton(Birmingham Women's Hospital), Elysa Marco, Tyhiesia Donald(St. George's University), C. Nowak(Boston Children's at Waltham), Hákon Hákonarson, Lars Kjærsgaard Hansen(Odense University Hospital), Élodie Adler(University of Washington), Richard Person(Baylor College of Medicine), Katherine R. Yearwood(St. George's University)
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