Persistent URL of this record https://hdl.handle.net/1887/3736259
Documents
-
- Download
- 399.full
- Publisher's Version
-
open access
- Full text at publishers site
In Collections
This item can be found in the following collections:
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals
- All authors
- Koene, S.; Ropers, F.G.; Wieland, J.; Rybak, T.; Wildschut, F.; Berghuis, D.; Morgan, A.; Trelles, M.P.; Scheepe, J.R.; Boekenkamp, R.; Peeters-Scholte, C.M.P.C.D.; Braden, R.; Santen, G.W.E.
- Date
- 2023-12-15
- Journal
- Journal of Medical Genetics
- Volume
- 61
- Issue
- 4
- Pages
- 399 - 404