Article info
Developmental defects
Original research
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome
- Correspondence to Professor Marcella Zollino, Genetica Medica, Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia, Roma 168, Italy; marcella.zollino{at}unicatt.it
Citation
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome
Publication history
- Received June 3, 2020
- Revised October 2, 2020
- Accepted November 26, 2020
- First published December 24, 2020.
Online issue publication
January 21, 2022
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- Previous version (15 January 2021).
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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.