Publications by authors named "Sabrina Classen"

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A novel inverted 17p13.3 microduplication disrupting PAFAH1B1 (LIS1) in a girl with syndromic lissencephaly.
Sabrina Classen, Timm Goecke, Matthias Drechsler, Beate Betz, Natalie Nickel

Am J Med Genet Aยท June 2013

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