Publications by authors named "Eva Wohlleber"

15Publications

Recurrent null mutation in SPG20 leads to Troyer syndrome.

Mol Cell Probes 2015 Oct 20;29(5):315-8. Epub 2015 May 20.

Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany; Centogene, Rostock, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.mcp.2015.05.006DOI Listing
October 2015

Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation.

Eur J Med Genet 2011 Jan-Feb;54(1):67-72. Epub 2010 Oct 13.

Institute of Human Genetics, University of Bonn, Biomedizinisches Zentrum, Sigmund-Freud-Strasse 25, D-53105 Bonn, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2010.09.012DOI Listing
June 2011