FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants
by Mitter, Diana (Author)
, Pringsheim, Milka (Author)
, Kaulisch, Marc (Author)
, Plümacher, Kim Sarah (Author)
, Schröder, Simone (Author)
, Warthemann, Rita (Author)
, Abou Jamra, Rami (Author)
, Baethmann, Martina (Author)
, Bast, Thomas (Author)
, Büttel, Hans-Martin (Author)
, Cohen, Julie S. (Author)
, Conover, Elizabeth (Author)
, Courage, Carolina (Author)
, Eger, Angelika (Author)
, Fatemi, Ali (Author)
, Grebe, Theresa A. (Author)
, Hauser, Natalie S. (Author)
, Heinritz, Wolfram (Author)
, Helbig, Katherine L. (Author)
, Heruth, Marion (Author)
, Huhle, Dagmar (Author)
, Höft, Karen (Author)
, Karch, Stephanie (Author)
, Kluger, Gerhard (Author)
, Korenke, Christoph (Author)
, Lemke, Johannes R. (Author)
, Lutz, Richard E. (Author)
, Patzer, Steffi (Author)
, Prehl, Isabelle (Author)
, Hoertnagel, Konstanze (Author)
, Ramsey, Keri (Author)
, Rating, Tina (Author)
, Rieß, Angelika (Author)
, Rohena, Luis (Author)
, Schimmel, Mareike (Author)
, Westman, Rachel (Author)
, Zech, Frank-Martin (Author)
, Zoll, Barbara (Author)
, Malzahn, Dörthe (Author)
, Zirn, Birgit (Author)
, Brockmann, Knut (Author)
,
Call Number:
Loading…
Located:
Loading…
Article (Journal)
Online Resource