De novo and biallelic DEAF1 variants cause a phenotypic spectrum
Maria João Nabais Sá(Radboud University Nijmegen), Anneke T. Vulto-vanSilfhout(Radboud University Nijmegen), Miranda Splitt(Newcastle upon Tyne Hospital), Edmund Cauley(George Washington University), Julián A. Martínez-Agosto(University of California, Los Angeles), Arjan P.M. de Brouwer(Radboud University Nijmegen), Stacey McGee(Southern Illinois University School of Medicine), Jeanne Amiel(Hôpital Necker-Enfants Malades), Heather C. Mefford(University of Washington), M. Chiara Manzini(Rutgers, The State University of New Jersey), Tyler Mark Pierson(National Human Genome Research Institute), John M. Graham(Cedars-Sinai Medical Center), Rani Sachdev(Victorian Clinical Genetics Services), Jan-Maarten Cobben(London North West Healthcare NHS Trust), Philip J. Jensik(Southern Illinois University School of Medicine), Christèle Dubourg(Centre Hospitalier Universitaire de Rennes), Elizabeth E. Palmer(The University of Sydney), Leonie A. Menke(Amsterdam University Medical Centers), Michael Parker(Wellcome Sanger Institute), Ehsan Ghayoor Karimiani(St George's, University of London), Bert B.A. de Vries(Radboud University Nijmegen), Nayana Lahiri(St George’s University Hospitals NHS Foundation Trust), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Naama Orenstein(Tel Aviv University), Delphine Héron(Sorbonne Université), Rachel Harrison(Nottingham University Hospitals NHS Trust), Evan McNeil(Beth Israel Deaconess Medical Center), Randi J. Hagerman(University of California Davis Medical Center), Jonathan Berg(King's College London), Roberto Colombo(University of Milan), Elysa J. Marco(Dominican University of California), Sylvie Odent(Centre National de la Recherche Scientifique), Boris Keren(Sorbonne Université), Hester Y. Kroes(University Medical Center Utrecht), Chanika Phornphutkul(Brown University), Tara Montgomery(Newcastle upon Tyne Hospital), Abbey Scott(Seattle Children's Hospital)
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