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
November 23, 2015
Article Versions
- Previous version (30 September 2015).
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