Clinical Epigenetics

, 8:40 | Cite as

Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes

  • Silvia Russo
  • Luciano Calzari
  • Alessandro Mussa
  • Ester Mainini
  • Matteo Cassina
  • Stefania Di Candia
  • Maurizio Clementi
  • Sara Guzzetti
  • Silvia Tabano
  • Monica Miozzo
  • Silvia Sirchia
  • Palma Finelli
  • Paolo Prontera
  • Silvia Maitz
  • Giovanni Sorge
  • Annalisa Calcagno
  • Mohamad Maghnie
  • Maria Teresa Divizia
  • Daniela Melis
  • Emanuela Manfredini
  • Giovanni Battista Ferrero
  • Vanna Pecile
  • Lidia Larizza
Open Access
Erratum

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.

Notes

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).

Reference

  1. 1.
    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.CrossRefPubMedPubMedCentralGoogle Scholar

Copyright information

© Russo et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  • Silvia Russo
    • 1
  • Luciano Calzari
    • 1
  • Alessandro Mussa
    • 2
  • Ester Mainini
    • 1
  • Matteo Cassina
    • 3
  • Stefania Di Candia
    • 4
  • Maurizio Clementi
    • 3
  • Sara Guzzetti
    • 1
  • Silvia Tabano
    • 5
  • Monica Miozzo
    • 5
  • Silvia Sirchia
    • 6
  • Palma Finelli
    • 1
  • Paolo Prontera
    • 7
  • Silvia Maitz
    • 8
  • Giovanni Sorge
    • 9
  • Annalisa Calcagno
    • 10
  • Mohamad Maghnie
    • 10
    • 15
  • Maria Teresa Divizia
    • 11
  • Daniela Melis
    • 12
  • Emanuela Manfredini
    • 13
  • Giovanni Battista Ferrero
    • 2
  • Vanna Pecile
    • 14
  • Lidia Larizza
    • 1
  1. 1.Human Molecular Genetics LaboratoryIRCCS Istituto Auxologico ItalianoMilanoItaly
  2. 2.Department of Pediatric and Public Health SciencesUniversity of TurinTorinoItaly
  3. 3.Clinical Genetics Unit, Department of Women’s and Children’s HealthUniversity of PaduaPadovaItaly
  4. 4.Department of PediatricsSan Raffaele Scientific InstituteMilanoItaly
  5. 5.Division of Pathology - Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Department of Pathophysiology and TransplantationUniversity of MilanMilanoItaly
  6. 6.Department of Health SciencesUniversity of MilanMilanoItaly
  7. 7.Medical Genetics Unit, Department of Surgical and Biomedical SciencesUniversity of Perugia, Hospital “S. M. della Misericordia”PerugiaItaly
  8. 8.Clinical Pediatric Genetics Unit, Pediatrics ClinicsMBBM Foundation, S. Gerardo HospitalMonzaItaly
  9. 9.Department of Pediatrics and Medical SciencesAO “Policlinico Vittorio Emanuele”CataniaItaly
  10. 10.Pediatric Endocrine Unit, Department of Pediatrics, IRCCSChildren’s Hospital Giannina GasliniGenovaItaly
  11. 11.Department of Medical Genetics, IRCCSChildren’s Hospital Giannina GasliniGenovaItaly
  12. 12.Clinical Pediatric Genetics, Department of PediatricsUniversity “Federico II”NapoliItaly
  13. 13.Medical Genetics Unit, Department of Laboratory MedicineNiguarda Ca’ Granda HospitalMilanoItaly
  14. 14.Institute for Maternal and Child HealthFoundation IRCCS Burlo Garofolo InstituteTriesteItaly
  15. 15.Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child HealthUniversity of GenovaGenovaItaly

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