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Publications by authors named "Ines Eger"

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Novel truncating PPM1D mutation in a patient with intellectual disability.
Joseph Porrmann, Andreas Rump, Karl Hackmann, Nataliya Di Donato, Anne-Karin Kahlert, Ines Eger

Eur J Med Genet· January 2019


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Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion.
Janine Lenk, Joseph Porrmann, Martin Smitka, Ines Eger, Evelin Schröck

Ophthalmic Genet· October 2018


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