Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?

  • Amanda Salem Brasil, Alexsandra C. Malaquias, Luciana Turolla Wanderley, Chong Ae Kim, José Eduardo Krieger, Alexander A. L. Jorge, Alexandre C. Pereira, Débora Romeo Bertola
  • Arquivos Brasileiros de Endocrinologia & Metabologia, November 2010, FapUNIFESP (SciELO)
  • DOI: 10.1590/s0004-27302010000800009

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The following have contributed to this page: Jose Krieger