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Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice
  1. Correspondence to:
 Dr D J Halliday, Department of Clinical Genetics, The Churchill Hospital, Old Road, Headington, Oxford OX3 7LJ, UK;
 penny{at}bioch.ox.ac.uk
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Citation

Halliday DJ, Hutchinson S, Lonie L, et al
Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice

Publication history

  • First published August 1, 2002.
Online issue publication 
April 27, 2016

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