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De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops

Document Type

Article

Author

De Koning, M.A.; Santen, G.W.E.; Suerink, M.; Pimienta Ramirez, P.A.; Han, X.; Finnell, R.H.; Lei, Y.; Haak, M.C.; Ruiterkamp-Versteeg, M.H.A.; De Leeuw, N.; Schatz, U.A.; Ortiz, J.U.; Shoukier, M.; Rieger-Fackeldey, E.; Van Duinen, S.G.; Klein, W.M.; Witlox, R.S.G.M.

Source

In: Journal of Medical Genetics. (Journal of Medical Genetics, 1 June 2024, 61(6):549-552)

Subject

Language

English

ISSN

14686244
00222593

Online Access

Full Text (BMJ Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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