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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Foxg1 Syndrome[original query]
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Annals of clinical and translational neurology 2019 4 6 (4): 655-668.
Pringsheim Milka, Mitter Diana, Schröder Simone, Warthemann Rita, Plümacher Kim, Kluger Gerhard, Baethmann Martina, Bast Thomas, Braun Sarah, Büttel Hans-Martin, Conover Elizabeth, Courage Carolina, Datta Alexandre N, Eger Angelika, Grebe Theresa A, Hasse-Wittmer Annette, Heruth Marion, Höft Karen, Kaindl Angela M, Karch Stephanie, Kautzky Torsten, Korenke Georg C, Kruse Bernd, Lutz Richard E, Omran Heymut, Patzer Steffi, Philippi Heike, Ramsey Keri, Rating Tina, Rieß Angelika, Schimmel Mareike, Westman Rachel, Zech Frank-Martin, Zirn Birgit, Ulmke Pauline A, Sokpor Godwin, Tuoc Tran, Leha Andreas, Staudt Martin, Brockmann Kn
Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome.
Seizure 2021 5 89 45-47.
Bai Yan, Yi Aiwen, Xin Jing, Xu Jiaxin, Huang Mingw
Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registry.
Orphanet journal of rare diseases 2023 6 18 (1): 149.
Elise Brimble, Kathryn G Reyes, Kopika Kuhathaas, Orrin Devinsky, Maura R Z Ruzhnikov, Xilma R Ortiz-Gonzalez, Ingrid Scheffer, Nadia Bahi-Buisson, Heather Olson,
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