May 05, 2009; 72 (18) NeuroImages
Medulloblastoma associated with novel PTCH mutation as primary manifestation of Gorlin syndrome
John R. Crawford, Brian R. Rood, Christopher T. Rossi, Gilbert Vezina
First published May 4, 2009, DOI: https://doi.org/10.1212/WNL.0b013e3181a413d6
John R. Crawford
Brian R. Rood
Christopher T. Rossi
Medulloblastoma associated with novel PTCH mutation as primary manifestation of Gorlin syndrome
John R. Crawford, Brian R. Rood, Christopher T. Rossi, Gilbert Vezina
Neurology May 2009, 72 (18) 1618; DOI: 10.1212/WNL.0b013e3181a413d6
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vol. 72 no. 18 1618
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History:
- First Published May 4, 2009.
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© 2009
Author Disclosures
- John R. Crawford, MD, MS,
- Brian R. Rood, MD,
- Christopher T. Rossi, MD and
- Gilbert Vezina, MD
- John R. Crawford, MD, MS,
- Brian R. Rood, MD,
- Christopher T. Rossi, MD and
- Gilbert Vezina, MD
- Washington, DC
- Address correspondence and reprint requests to Dr. John R. Crawford, Department of Neurology, Children's National Medical Center, The George Washington University, Washington, DC 20010; jcrawfor{at}cnmc.org
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