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Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
- 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
Citation
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
April 27, 2016
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2008 BMJ Publishing Group Ltd