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Cited In for PubMed (Select 9475610)


Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population.

McMaster ML, Goldstein AM, Parry DM.

J Med Genet. 2011 Jul;48(7):444-9. doi: 10.1136/jmg.2010.085092. Epub 2011 Jan 25.


Chordoma in the lateral medullary cistern in a patient with tuberous sclerosis: A case report and review of the literature.

Kimmell KT, Dayoub H, Stolzenberg ED, Sincoff EH.

Surg Neurol Int. 2010 May 31;1:13. doi: 10.4103/2152-7806.63908.


Update on the cytogenetics and molecular genetics of chordoma.

Larizza L, Mortini P, Riva P.

Hered Cancer Clin Pract. 2005 Feb 15;3(1):29-41. doi: 10.1186/1897-4287-3-1-29.


Aberrant hyperactivation of akt and Mammalian target of rapamycin complex 1 signaling in sporadic chordomas.

Han S, Polizzano C, Nielsen GP, Hornicek FJ, Rosenberg AE, Ramesh V.

Clin Cancer Res. 2009 Mar 15;15(6):1940-6. doi: 10.1158/1078-0432.CCR-08-2364. Epub 2009 Mar 10.


Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33.

Kelley MJ, Korczak JF, Sheridan E, Yang X, Goldstein AM, Parry DM.

Am J Hum Genet. 2001 Aug;69(2):454-60. Epub 2001 Jul 10.

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