Recurrent duplications of 17q12 associated with variable phenotypes
Year: 2015
Type: article
Study design: Observational Study
DOI: 10.1002/ajmg.a.37351
Authors: Elyse Mitchell, Andrew Douglas, Susanne Kjaegaard, Bert Callewaert, Arnaud Vanlander, Sandra Janssens, Amy Lawson Yuen, Cindy Skinner, Pinella Failla, Antonino Alberti, Emanuela Avola, Marco Fichera, Maria Kibaek, Maria C. Digilio, Mark C. Hannibal, Nicolette S. den Hollander, Veronica Bizzarri, Alessandra Renieri, Maria Antonietta Mencarelli, Tomas Fitzgerald, Serena Piazzolla, Elke van Oudenhove, Corrado Romano, Charles Schwartz, Evan E. Eichler, Anne Slavotinek, Luis Escobar, Diana Rajan, John Crolla, Nigel Carter, Jennelle C. Hodge, Heather C. Mefford
Institutions: Mayo Clinic, Princess Anne Hospital, Copenhagen University Hospital, Rigshospitalet, Ghent University, MultiCare Health System, Greenwood Genetic Center, I.R.C.C.S. Oasi Maria SS, University of Catania, Odense University Hospital, Bambino Gesù Children's Hospital, University of Michigan, Michigan Medicine, Leiden University Medical Center, University of Siena, Wellcome Sanger Institute, Howard Hughes Medical Institute, University of Washington, University of California, San Francisco, Salisbury District Hospital, Wessex Regional Genetics Laboratory, Cedars-Sinai Medical Center, Seattle Children's Hospital
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2163482548