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Li, V. FOXG1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5571 (accessed on 21 September 2026).
Li V. FOXG1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5571. Accessed September 21, 2026.
Li, Vivi. "FOXG1 Gene" Encyclopedia, https://encyclopedia.pub/entry/5571 (accessed September 21, 2026).
Li, V. (2020, December 25). FOXG1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5571
Li, Vivi. "FOXG1 Gene." Encyclopedia. Web. 25 December, 2020.
FOXG1 Gene
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Forkhead box G1

genes

References

  1. Brunetti-Pierri N, Paciorkowski AR, Ciccone R, Della Mina E, Bonaglia MC,Borgatti R, Schaaf CP, Sutton VR, Xia Z, Jelluma N, Ruivenkamp C, Bertrand M, de Ravel TJ, Jayakar P, Belli S, Rocchetti K, Pantaleoni C, D'Arrigo S, Hughes J,Cheung SW, Zuffardi O, Stankiewicz P. Duplications of FOXG1 in 14q12 areassociated with developmental epilepsy, mental retardation, and severe speechimpairment. Eur J Hum Genet. 2011 Jan;19(1):102-7. doi: 10.1038/ejhg.2010.142.
  2. De Filippis R, Pancrazi L, Bjørgo K, Rosseto A, Kleefstra T, Grillo E,Panighini A, Cardarelli F, Meloni I, Ariani F, Mencarelli MA, Hayek J, Renieri A,Costa M, Mari F. Expanding the phenotype associated with FOXG1 mutations and invivo FoxG1 chromatin-binding dynamics. Clin Genet. 2012 Oct;82(4):395-403. doi:10.1111/j.1399-0004.2011.01810.x.
  3. Florian C, Bahi-Buisson N, Bienvenu T. FOXG1-Related Disorders: From Clinical Description to Molecular Genetics. Mol Syndromol. 2012 Apr;2(3-5):153-163.
  4. Kortüm F, Das S, Flindt M, Morris-Rosendahl DJ, Stefanova I, Goldstein A, HornD, Klopocki E, Kluger G, Martin P, Rauch A, Roumer A, Saitta S, Walsh LE,Wieczorek D, Uyanik G, Kutsche K, Dobyns WB. The core FOXG1 syndrome phenotypeconsists of postnatal microcephaly, severe mental retardation, absent language,dyskinesia, and corpus callosum hypogenesis. J Med Genet. 2011 Jun;48(6):396-406.doi: 10.1136/jmg.2010.087528.
  5. Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R,Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B,Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F,Renieri A. Novel FOXG1 mutations associated with the congenital variant of Rettsyndrome. J Med Genet. 2010 Jan;47(1):49-53. doi: 10.1136/jmg.2009.067884.
  6. Striano P, Paravidino R, Sicca F, Chiurazzi P, Gimelli S, Coppola A, Robbiano A, Traverso M, Pintaudi M, Giovannini S, Operto F, Vigliano P, Granata T, CoppolaG, Romeo A, Specchio N, Giordano L, Osborne LR, Gimelli G, Minetti C, Zara F.West syndrome associated with 14q12 duplications harboring FOXG1. Neurology. 2011May 3;76(18):1600-2. doi: 10.1212/WNL.0b013e3182194bbf.
  7. Tohyama J, Yamamoto T, Hosoki K, Nagasaki K, Akasaka N, Ohashi T, Kobayashi Y,Saitoh S. West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14. Am J Med Genet A. 2011Oct;155A(10):2584-8. doi: 10.1002/ajmg.a.34224.
  8. Yeung A, Bruno D, Scheffer IE, Carranza D, Burgess T, Slater HR, Amor DJ. 4.45Mb microduplication in chromosome band 14q12 including FOXG1 in a girl withrefractory epilepsy and intellectual impairment. Eur J Med Genet. 2009Nov-Dec;52(6):440-2. doi: 10.1016/j.ejmg.2009.09.004.
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