Corrigendum to "Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders" [Gene 706 (2019) 162-171]

Affiliations

¹ Unit of Medical Genetics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
² Unit of Pediatrics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
³ Unit of Medical Genetics, AUSL Romagna, Cesena, Italy.
⁴ Unit of Medical Genetics, University of Parma, Parma, Italy.
⁵ IRCCS Istituto delle Scienze Neurologiche di Bologna, Bellaria Hospital, Bologna, Italy.
⁶ Child Neurology Unit, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
⁷ Unit of Medical Genetics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. Electronic address: claudio.graziano@unibo.it.

Published Erratum

Pamela Magini et al. Gene. 2020.

. 2020 Apr 20:735:144393.

doi: 10.1016/j.gene.2020.144393. Epub 2020 Feb 6.

¹ Unit of Medical Genetics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
² Unit of Pediatrics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
³ Unit of Medical Genetics, AUSL Romagna, Cesena, Italy.
⁴ Unit of Medical Genetics, University of Parma, Parma, Italy.
⁵ IRCCS Istituto delle Scienze Neurologiche di Bologna, Bellaria Hospital, Bologna, Italy.
⁶ Child Neurology Unit, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
⁷ Unit of Medical Genetics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. Electronic address: claudio.graziano@unibo.it.

No abstract available

Erratum for

Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders.
Magini P, Scarano E, Donati I, Sensi A, Mazzanti L, Perri A, Tamburrino F, Mongelli P, Percesepe A, Visconti P, Parmeggiani A, Seri M, Graziano C. Magini P, et al. Gene. 2019 Jul 20;706:162-171. doi: 10.1016/j.gene.2019.05.007. Epub 2019 May 11. Gene. 2019. PMID: 31085274