Persistent URL of this record https://hdl.handle.net/1887/3721007
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De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops
- All authors
- Koning, M.A. de; Ramirez, P.A.P.; Haak, M.C.; Han, X.; Ruiterkamp-Versteeg, M.H.; Leeuw, N. de; Schatz, U.A.; Shoukier, M.; Rieger-Fackeldey, E.; Ortiz, J.U.; Duinen, S.G. van; Klein, W.M.; Witlox, R.S.G.M.; Finnell, R.H.; Santen, G.W.E.; Lei, Y.P.; Suerink, M.
- Date
- 2024-01-25
- Journal
- Journal of Medical Genetics