Toggle Main Menu Toggle Search

Open Access padlockePrints

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

Lookup NU author(s): Dr Helen Simpson, Dr Stephen Ball


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.

Publication metadata

Author(s): Clowes VE, Shaw-Smith C, Simpson H, Ball SG, Acerini CL

Publication type: Letter

Publication status: Published

Journal: Clinical Endocrinology

Year: 2008

Volume: 68

Issue: 4

Pages: 666-667

ISSN (print): 0300-0664

ISSN (electronic): 1365-2265


DOI: 10.1111/j.1365-2265.2007.03056.x