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No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome
Benjamin Abo-Dalo, Melanie Roes, Sonia Canún, Martin Delatycki, Gabriele Gillessen-Kaesbach, Ihor Hrytsiuk, Christine Jung, Bronwyn Kerr, David Mowat, Eva Seemanova, Carlos E. Steiner, Helen Stewart, Patrick Thierry, Griet Van Buggenhout, Sue White, Martin Zenker, Kerstin Kutsche*
*Corresponding author for this work
- University Hospital Hamburg-Eppendorf
- Medical Genetics Division
- Royal Children's Hospital
- Lviv Specialized Children's Hospital
- Ruprecht-Karls Universität Heidelberg
- St Mary's Hospital London
- Sydney Children's Hospital
- Charles University
- State University of Campinas (Unicamp)
- Department of Cardiovascular Medicine
- Hospital C.H.I.
- KU Leuven
- Genetic Health Services Victoria
- University of Erlangen–Nuremberg
8
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(Scopus)