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Results: 5

Cited In for PubMed (Select 9475610)

1.

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.

2.

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.

3.

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.

4.

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.

5.

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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