Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.

Translated title of the contribution: Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
  • W.W. de Leng
  • , M. Jansen
  • , R. Carvalho
  • , M. Polak
  • , A.R. Musler
  • , A.N. Milne
  • , J.J. Keller
  • , F.H. Menko
  • , F.W.M. de Rooij
  • , C.A. Iacobuzio-Donahue
  • , F.M. Giardiello
  • , M.A.J. Weterman
  • , G. Johan A. Offerhaus

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionGenetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
Original languageUndefined/Unknown
Pages (from-to)568-573
Number of pages6
JournalClinical Genetics
Volume72
Issue number6
Publication statusPublished - 2007

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