Article info
PDFGenotype-phenotype correlations
Original article
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype–phenotype correlations in a large cohort of patients
- Correspondence to Professor Marcella Zollino, MD, Istituto di Genetica Medica, Università Cattolica Sacro Cuore, Largo F. Vito, 1 00168 Roma, Italy; mzollino{at}rm.unicatt.it
Citation
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype–phenotype correlations in a large cohort of patients
Publication history
- Received April 22, 2015
- Revised July 16, 2015
- Accepted July 28, 2015
- First published September 30, 2015.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
- You are viewing the most recent version of this article.
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.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/