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FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
Genet Med. 2018 Jan;20(1):98-108. doi: 10.1038/gim.2017.75. Epub 2017 Jun 29.
Genet Med. 2018.
PMID: 28661489
Free article.
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Pringsheim M, Mitter D, Schröder S, Warthemann R, Plümacher K, Kluger G, Baethmann M, Bast T, Braun S, Büttel HM, Conover E, Courage C, Datta AN, Eger A, Grebe TA, Hasse-Wittmer A, Heruth M, Höft K, Kaindl AM, Karch S, Kautzky T, Korenke GC, Kruse B, Lutz RE, Omran H, Patzer S, Philippi H, Ramsey K, Rating T, Rieß A, Schimmel M, Westman R, Zech FM, Zirn B, Ulmke PA, Sokpor G, Tuoc T, Leha A, Staudt M, Brockmann K.
Pringsheim M, et al.
Ann Clin Transl Neurol. 2019 Mar 3;6(4):655-668. doi: 10.1002/acn3.735. eCollection 2019 Apr.
Ann Clin Transl Neurol. 2019.
PMID: 31019990
Free PMC article.
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Expectoration of bronchial casts in association with Ramipril treatment.
Plümacher KS, Paul T, Sigler M.
Plümacher KS, et al.
Cardiol Young. 2019 Dec;29(12):1565-1566. doi: 10.1017/S1047951119002294. Epub 2019 Oct 9.
Cardiol Young. 2019.
PMID: 31594552
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