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The Koolen-de Vries syndrome: A phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant
David A. Koolen*, Rolph Pfundt, Katrin Linda, Gea Beunders, Hermine E. Veenstra-Knol, Essie H. Conta, Ana Maria Fortuna, Gabriele Gillessen-Kaesbach, Sarah Dugan, Sara Halbach, Omar A. Abdul-Rahman, Heather M. Winesett, Wendy K. Chung, Marguerite Dalton, Petia S. Dimova, Teresa Mattina, Katrina Prescott, Hui Z. Zhang, Howard M. Saal, Jayne Y. Hehir-Kwa
*Corresponding author for this work
- Radboud University Nijmegen
- University of Amsterdam
- University of Groningen
- Seattle Children's Hospital
- University of Chicago
- University of Mississippi
- Columbia University in the City of New York
- Auckland District Health Board and Counties Manukau District Health Board
- University Hospital St. Naum
- University of Catania
- Yorkshire Regional Genetics Service
- Yale University
- University of Cincinnati
- University of Antwerp
- IRCCS Oasi Maria SS. - Troina (EN)
- Erasmus University Medical Center
- Leiden University
- Cambridge University Hospitals NHS Foundation Trust
- University of Tartu
- University of California, San Diego
- Nottingham University Hospitals NHS Trust
- Newcastle University
- The University of Queensland
- Washington University in St. Louis
- University of Cantabria
- University of Adelaide
- University of Washington, Seattle
45
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