MEN2 screening dilemmas in a family with a novel RET mutation in the MEN2 susceptibility region of the gene, a family history of Hirschsprung disease, and no family history of MEN2-related tumours

  1. Lookup NU author(s)
  2. Dr Helen Simpson
  3. Dr Stephen Ball
Author(s)Clowes VE, Shaw-Smith C, Simpson H, Ball SG, Acerini CL
Publication type Letter
JournalClinical Endocrinology
Year2008
Volume68
Issue4
Pages666-667
ISSN (print)0300-0664
ISSN (electronic)1365-2265
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URLhttp://dx.doi.org/10.1111/j.1365-2265.2007.03056.x
DOI10.1111/j.1365-2265.2007.03056.x
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