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Xu, C. Gorlin-Chaudhry-Moss Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4046 (accessed on 25 September 2026).
Xu C. Gorlin-Chaudhry-Moss Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4046. Accessed September 25, 2026.
Xu, Camila. "Gorlin-Chaudhry-Moss Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4046 (accessed September 25, 2026).
Xu, C. (2020, December 23). Gorlin-Chaudhry-Moss Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4046
Xu, Camila. "Gorlin-Chaudhry-Moss Syndrome." Encyclopedia. Web. 23 December, 2020.
Gorlin-Chaudhry-Moss Syndrome
Edit

Gorlin-Chaudhry-Moss syndrome is a condition that affects many parts of the body. The signs and symptoms of this disorder are apparent from birth or infancy.

genetic conditions

References

  1. Aravena T, Passalacqua C, Pizarro O, Aracena M. Two sisters resemblingGorlin-Chaudhry-Moss syndrome. Am J Med Genet A. 2011 Oct;155A(10):2552-5. doi:10.1002/ajmg.a.34204.
  2. Ehmke N, Graul-Neumann L, Smorag L, Koenig R, Segebrecht L, Magoulas P,Scaglia F, Kilic E, Hennig AF, Adolphs N, Saha N, Fauler B, Kalscheuer VM, HennigF, Altmüller J, Netzer C, Thiele H, Nürnberg P, Yigit G, Jäger M, Hecht J, KrügerU, Mielke T, Krawitz PM, Horn D, Schuelke M, Mundlos S, Bacino CA, Bonnen PE,Wollnik B, Fischer-Zirnsak B, Kornak U. De Novo Mutations in SLC25A24 Cause aCraniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, andMitochondrial Dysfunction. Am J Hum Genet. 2017 Nov 2;101(5):833-843. doi:10.1016/j.ajhg.2017.09.016.
  3. Rosti RO, Karaer K, Karaman B, Torun D, Guran S, Bahce M. Gorlin-Chaudhry-Mosssyndrome revisited: expanding the phenotype. Am J Med Genet A. 2013Jul;161A(7):1737-42. doi: 10.1002/ajmg.a.35954.
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Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
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Entry Collection: MedlinePlus
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Update Date: 23 Dec 2020
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