Article info

other Versions

PDF
Original article
Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature

Authors

  1. * Correspondence to
    Dr Meena Balasubramanian, Sheffield Clinical Genetics Service, Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield S10 2TH, UK; meena.balasubramanian{at}nhs.net
View Full Text

Citation

Balasubramanian M, Willoughby J, Fry AE, et al
Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature

Publication history

  • Received 7 October 2016
  • Revised 6 December 2016
  • Accepted 12 December 2016
  • Published online 18 January 2017.

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.