Jaffe-Campanacci syndrome, revisited: Detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

  • Douglas R. Stewart
  • , Hilde Brems
  • , Alicia G. Gomes
  • , Sarah L. Ruppert
  • , Tom Callens
  • , Jennifer Williams
  • , Kathleen Claes
  • , Michael B. Bober
  • , Rachel Hachen
  • , Leonard B. Kaban
  • , Hua Li
  • , Angela Lin
  • , Marie McDonald
  • , Serge Melancon
  • , June Ortenberg
  • , Heather B. Radtke
  • , Ignace Samson
  • , Robert A. Saul
  • , Joseph Shen
  • , Elizabeth Siqveland
    • Tomi L. Toler, Merel Van Maarle, Margaret Wallace, Misti Williams, Eric Legius, Ludwine Messiaen

Research output: Contribution to journal › Article › peer-review

40 Scopus citations

Fingerprint

Dive into the research topics of 'Jaffe-Campanacci syndrome, revisited: Detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder'. Together they form a unique fingerprint.

Keyphrases

Medicine and Dentistry