Silke Pauli

Years Active: 2017-2020
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Roser Ufartes, Hanna Berger, Katharina Till, Gabriela Salinas, Marc Sturm, Janine Altmüller, Peter Nürnberg, Holger Thiele, Rudolf Funke, Neophytos Apeshiotis, Hendrik Langen, Bernd Wollnik, Annette Borchers, Silke Pauli
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome. Human genetics 139 (11) (2020)
Silke Pauli, Ruchi Bajpai, Annette Borchers
CHARGEd with neural crest defects. American journal of medical genetics. Part C, Seminars in medical genetics 175 (4) (2017)

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