De novo and biallelic DEAF1 variants cause a phenotypic spectrum
Titel:
De novo and biallelic DEAF1 variants cause a phenotypic spectrum
Auteur:
Nabais Sá, Maria J. Jensik, Philip J. McGee, Stacey R. Parker, Michael J. Lahiri, Nayana McNeil, Evan P. Kroes, Hester Y. Hagerman, Randi J. Harrison, Rachel E. Montgomery, Tara Splitt, Miranda Palmer, Elizabeth E. Sachdev, Rani K. Mefford, Heather C. Scott, Abbey A. Martinez-Agosto, Julian A. Lorenz, Rüdiger Orenstein, Naama Berg, Jonathan N. Amiel, Jeanne Heron, Delphine Keren, Boris Cobben, Jan-Maarten Menke, Leonie A. Marco, Elysa J. Graham Jr, John M. Pierson, Tyler Mark Karimiani, Ehsan Ghayoor Maroofian, Reza Manzini, M. Chiara Cauley, Edmund S. Colombo, Roberto Odent, Sylvie Dubourg, Christele Phornphutkul, Chanika de Brouwer, Arjan P.M. de Vries, Bert B.A. Vulto-vanSilfhout, Anneke T.