Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations
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author: Bert Callewaert, Bart L Loeys, Eloisa Arbustini, Peter Robinson, Julie De Backer, Christophe Beroud, Catherine Boileau, Mireille Claustres, Gwenaëlle Collod-Béroud, Claire Bonithon-Kopp, Alice Masurel-Paulet
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