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FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants
2017
109 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
7.05
FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants | Researchclopedia
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University Hospital Leipzig
Martina Baethmann
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München Klinik
Thomas Bast
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Diakonie Kork
Hans-Martin Büttel
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SLK-Kliniken Heilbronn
Julie S. Cohen
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Kennedy Krieger Institute
Elizabeth Conover
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University of Nebraska Medical Center
Carolina Courage
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University of Bern
Angelika Eger
Ali Fatemi
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Kennedy Krieger Institute
Theresa A. Grebe
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Phoenix Children's Hospital
Natalie Hauser
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Inova Fairfax Hospital
Wolfram Heinritz
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Praxis für Humangenetik
Katherine L. Helbig
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Ambry Genetics (United States)
Marion Heruth
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Sana Kliniken Leipziger Land
Dagmar Huhle
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Praxis für Humangenetik
Karen Höft
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Klinikum Magdeburg
Stephanie Karch
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University Hospital Heidelberg
Gerhard Kluger
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Schön Klinik Vogtareuth
Georg Christoph Korenke
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Klinikum Oldenburg
Johannes R. Lemke
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University Hospital Leipzig
Richard E. Lutz
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University of Nebraska Medical Center
Steffi Patzer
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Krankenhaus St. Elisabeth und St. Barbara
Isabelle Prehl
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CeGaT (Germany)
Konstanze Hoertnagel
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CeGaT (Germany)
Keri Ramsey
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Translational Genomics Research Institute
Tina Rating
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Klinikum Bremen-Mitte
Angelika Rieß
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Universitätsklinikum Tübingen
Luis Rohena
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San Antonio Military Medical Center
Mareike Schimmel
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University Hospital Augsburg
Rachel Westman
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St. Luke's Children's Hospital
Frank-Martin Zech
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Brüderkrankenhaus St. Josef Paderborn
Barbara Zoll
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Universitätsmedizin Göttingen
Dörthe Malzahn
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University of Göttingen
Birgit Zirn
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Genetikum
Knut Brockmann
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Universitätsmedizin Göttingen