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Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
  1. Dr L Faivre, Centre de Génétique, Hôpital d’Enfants, 10, bd Maréchal De Lattre de Tassigny, 21034 Dijon, France; laurence.faivre{at}chu-dijon.fr
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Faivre L, Collod-Beroud G, Child A, et al
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

Publication history

  • Received November 20, 2007
  • Revised January 25, 2008
  • Accepted February 2, 2008
  • First published February 29, 2008.
Online issue publication 
June 02, 2008

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