Publications by authors named "Celine B Gerber"

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De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay.
Thoa Ha, Angela Morgan, Meghan N Bartos, Katelyn Beatty, Benjamin Cogné, Céline B Gerber

Am J Med Genet A· July 2024

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Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6.
Céline B Gerber, Anna Fliedner, Oliver Bartsch, Siren Berland, Malin Dewenter

Clin Genet· September 2022

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