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Gorlin syndrome
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References
These sources were used to develop the Genetics Home Reference
condition summary
on Gorlin syndrome.
Bale AE, Yu KP. The hedgehog pathway and basal cell carcinomas. Hum Mol Genet. 2001 Apr;10(7):757-62. Review.
PubMed citation
Evans DG, Howard E, Giblin C, Clancy T, Spencer H, Huson SM, Lalloo F. Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service. Am J Med Genet A. 2010 Feb;152A(2):327-32. doi: 10.1002/ajmg.a.33139.
PubMed citation
Gene Review: Nevoid Basal Cell Carcinoma
Syndrome
Gorlin RJ. Nevoid basal cell carcinoma (Gorlin) syndrome. Genet Med. 2004 Nov-Dec;6(6):530-9. Review.
PubMed citation
High A, Zedan W. Basal cell nevus syndrome. Curr Opin Oncol. 2005 Mar;17(2):160-6. Review.
PubMed citation
Lo Muzio L, Pastorino L, Levanat S, Musani V, Situm M, Scarra GB. Clinical utility gene card for: Gorlin syndrome. Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.9. Epub 2011 Feb 9.
PubMed citation
Madras J, Lapointe H. Keratocystic odontogenic tumour: reclassification of the odontogenic keratocyst from cyst to tumour. J Can Dent Assoc. 2008 Mar;74(2):165-165h.
PubMed citation
Muller EA, Aradhya S, Atkin JF, Carmany EP, Elliott AM, Chudley AE, Clark RD, Everman DB, Garner S, Hall BD, Herman GE, Kivuva E, Ramanathan S, Stevenson DA, Stockton DW, Hudgins L. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. Am J Med Genet A. 2012 Feb;158A(2):391-9. doi: 10.1002/ajmg.a.34216. Epub 2011 Dec 21.
PubMed citation
Reviewed: October 2012
Published: May 13, 2013
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