FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants

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FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants

Author: Mitter, Diana; Pringsheim, Milka; Kaulisch, Marc; Pluemacher, Kim Sarah; Schroeder, Simone; Warthemann, Rita; Abou Jamra, Rami; Baethmann, Martina; Bast, Thomas; Buettel, Hans-Martin; Cohen, Julie S.; Conover, Elizabeth; Courage, Carolina; Eger, Angelika; Fatemi, Ali; Grebe, Theresa A.; Hauser, Natalie S.; Heinritz, Wolfram; Helbig, Katherine L.; Heruth, Marion; Huhle, Dagmar; Hoeft, Karen; Karch, Stephanie; Kluger, Gerhard; Korenke, G. Christoph; Lemke, Johannes R.; Lutz, Richard E.; Patzer, Steffi; Prehl, Isabelle; Hoertnagel, Konstanze; Ramsey, Keri; Rating, Tina; Riess, Angelika; Rohena, Luis; Schimmel, Mareike; Westman, Rachel; Zech, Frank-Martin; Zoll, Barbara; Malzahn, Dorthe; Zirn, Birgit; Brockmann, Knut
Tübinger Autor(en):
Riess, Angelika
Published in: Genetics in Medicine (2018), Bd. 20, H. 1, S. 98-108
Verlagsangabe: Nature Publishing Group
Language: English
Full text: http://dx.doi.org/10.1038/gim.2017.75
ISSN: 1530-0366
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
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