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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
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Brian R. Rood
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Citation
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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Article Information

vol. 72 no. 18 1618
DOI: 
https://doi.org/10.1212/WNL.0b013e3181a413d6
PubMed: 
19414732

Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published May 4, 2009.

Copyright & Usage: 
© 2009

Author Disclosures

    1. John R. Crawford, MD, MS,
    2. Brian R. Rood, MD,
    3. Christopher T. Rossi, MD and
    4. Gilbert Vezina, MD
  1. John R. Crawford, MD, MS,
  2. Brian R. Rood, MD,
  3. Christopher T. Rossi, MD and
  4. Gilbert Vezina, MD
  1. Washington, DC
  1. 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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Article usage: May 2009 to December 2022

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