Cover Image, Volume 170A, Number 7, July 2016
Elisa Giorgio
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorAndrea Ciolfi
Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù IRCSS, Rome, Italy
Centro di Ricerca per gli alimenti e la nutrizione, CREA, Rome, Italy
Search for more papers by this authorElisa Biamino
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorViviana Caputo
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy
Search for more papers by this authorEleonora Di Gregorio
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Search for more papers by this authorElga Fabia Belligni
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorAlessandro Calcia
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorElena Gaidolfi
Centro Diagnostico Cernaia, Magnetic Resonance Unit, Turin, Italy
Search for more papers by this authorAlessandro Bruselles
Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy
Search for more papers by this authorCecilia Mancini
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorSimona Cavalieri
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Search for more papers by this authorCristina Molinatto
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorMargherita Cirillo Silengo
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorGiovanni Battista Ferrero
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorMarco Tartaglia
Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù IRCSS, Rome, Italy
Search for more papers by this authorCorresponding Author
Alfredo Brusco
Department of Medical Sciences, University of Torino, Turin, Italy
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Correspondence to:
Alfredo Brusco, Ph.D., Department of Medical Sciences, University of Torino, via Santena 19, 10126, Torino, Italy.
E-mail: [email protected]
Search for more papers by this authorElisa Giorgio
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorAndrea Ciolfi
Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù IRCSS, Rome, Italy
Centro di Ricerca per gli alimenti e la nutrizione, CREA, Rome, Italy
Search for more papers by this authorElisa Biamino
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorViviana Caputo
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy
Search for more papers by this authorEleonora Di Gregorio
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Search for more papers by this authorElga Fabia Belligni
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorAlessandro Calcia
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorElena Gaidolfi
Centro Diagnostico Cernaia, Magnetic Resonance Unit, Turin, Italy
Search for more papers by this authorAlessandro Bruselles
Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy
Search for more papers by this authorCecilia Mancini
Department of Medical Sciences, University of Torino, Turin, Italy
Search for more papers by this authorSimona Cavalieri
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Search for more papers by this authorCristina Molinatto
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorMargherita Cirillo Silengo
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorGiovanni Battista Ferrero
Department of Public Health and Pediatrics, University of Torino, Turin, Italy
Search for more papers by this authorMarco Tartaglia
Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù IRCSS, Rome, Italy
Search for more papers by this authorCorresponding Author
Alfredo Brusco
Department of Medical Sciences, University of Torino, Turin, Italy
Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy
Correspondence to:
Alfredo Brusco, Ph.D., Department of Medical Sciences, University of Torino, via Santena 19, 10126, Torino, Italy.
E-mail: [email protected]
Search for more papers by this authorGraphical Abstract
The cover image, by Alfredo Brusco et al., is based on the Original Article Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain signifi cance: Two proof-of-concept examples, DOI: 10.1002/ajmg.a.37649.
