Erratum
Unfortunately, the original version of this article [1] contained two errors. Within the “Acknowledgements” section, the funding information was missing, and the second affiliation for Mohamad Maghnie was missing. The correct author list and “Acknowledgements” section are included in this erratum.
Reference
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, et al. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Clin Epigenetics. 2016;8:23. doi:10.1186/s13148-016-0183-8.
Acknowledgements
The authors thank the children and their families for participating in this study, the Beckwith–Wiedemann Syndrome Italian Association (AIBWS), the Silver–Russell Syndrome Italian Association (AISRS), and the following medical geneticists/clinicians for providing cases included among those herein described: Bedeschi MF (Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano), Donti E (Medical Genetics, Hospital Santa Maria della Misericordia, University of Perugia), Giordano L (City Hospital, Brescia), Lapi E (Meyer Children’s University Hospital, Firenze), Micaglio E (University Hospital, Padova), Neri M (S. Anna University Hospital, Ferrara), Rubinato E (University of Trieste), Vaccari R (Niguarda Hospital, Milano), and Pilotta A (City Hospital, Brescia).
The research was funded by MIUR PRIN 2009-2010 (to Lidia Larizza) and by a Ministry of Health “Ricerca Corrente” Grant to Istituto Auxologico Italiano IRCSS n 08C207_2012 (to Silvia Russo). Lidia Larizza and Silvia Russo are members of COST Action BM1208 “European Network for Human Congenital Imprinting Disorders” (http://www.cost.eu/COST_Actions/bmbs/BM1208).
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The online version of the original article can be found under doi:10.1186/s13148-016-0183-8.
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Russo, S., Calzari, L., Mussa, A. et al. Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Clin Epigenet 8, 40 (2016). https://doi.org/10.1186/s13148-016-0206-5
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DOI: https://doi.org/10.1186/s13148-016-0206-5